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 ATP6V0A1:
 
NM_001130020
Mutation details:
9
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NM_001130021
Mutation details:
9
records
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NM_005177
Mutation details:
9
records
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