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 SLC35G2:
 
NM_001097599
Mutation details:
8
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NM_001097600
Mutation details:
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NM_025246
Mutation details:
8
records
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