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 FBXW7:
 
NM_001013415
Mutation details:
93
records
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NM_018315
Mutation details:
95
records
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NM_033632
Mutation details:
102
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102
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NM_001257069
Mutation details:
9
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9
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