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 TAL1:
 
NM_001287347
Mutation details:
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NM_001290403
Mutation details:
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NM_001290404
Mutation details:
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NM_001290405
Mutation details:
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NM_003189
Mutation details:
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NM_001290406
No image for this transcript.
Mutation details:
1
records
Showing
1
-
10
/
1
mutation records.
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1
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1
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