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 THPO:
 
NM_000460
Mutation details:
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NM_001177597
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Mutation details:
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NM_001289998
Mutation details:
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NM_001290003
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NM_001290022
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NM_001290028
Mutation details:
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NM_001177598
No image for this transcript.
Mutation details:
2
records
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1
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10
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2
mutation records.
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NM_001289997
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Mutation details:
2
records
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2
mutation records.
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NM_001290026
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Mutation details:
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NM_001290027
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Mutation details:
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mutation records.
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