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 SLC52A2:
NM_001253815
Mutation details:
7
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NM_001253816
Mutation details:
7
records
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NM_024531
Mutation details:
7
records
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