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 CEP57L1:
 
NM_001083535
Mutation details:
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NM_001271852
Mutation details:
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NM_001271853
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Mutation details:
4
records
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4
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NM_173830
Mutation details:
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