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 PTPRC:
 
NM_002838
Mutation details:
29
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NM_080921
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Mutation details:
25
records
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NM_001267798
Mutation details:
3
records
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