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 SIRT1:
 
NM_001142498
Mutation details:
5
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NM_001314049
Mutation details:
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NM_012238
Mutation details:
5
records
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