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 MAP3K13:
 
NM_001242314
Mutation details:
12
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NM_004721
Mutation details:
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NM_001242317
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Mutation details:
9
records
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