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 PLCE1:
 
NM_001165979
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Mutation details:
37
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NM_001288989
Mutation details:
41
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NM_016341
Mutation details:
41
records
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