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 SUPT5H:
 
NM_001111020
Mutation details:
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NM_001130824
Mutation details:
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NM_001130825
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Mutation details:
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NM_003169
Mutation details:
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