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 CHST4:
NM_001166395
Mutation details:
5
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NM_005769
Mutation details:
5
records
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1
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10
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5
mutation records.
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1
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