ESCCdb: An Integrated Database for Esophageal Squamous Cell Carcinoma
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Consensus DEGs
Recurrent Mutations
Significant CNV
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Somatic mutations of GHR:
 
NM_000163
Mutation details:
15
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15
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NM_001242399
Mutation details:
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NM_001242400
Mutation details:
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NM_001242401
Mutation details:
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NM_001242402
Mutation details:
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NM_001242403
Mutation details:
15
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NM_001242404
Mutation details:
15
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15
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NM_001242405
Mutation details:
15
records
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15
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NM_001242406
Mutation details:
15
records
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10
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15
mutation records.
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NM_001242462
Mutation details:
10
records
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10
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10
mutation records.
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NM_001242460
No image for this transcript.
Mutation details:
14
records
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1
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10
/
14
mutation records.
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