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 NMNAT1:
NM_001297778
Mutation details:
2
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NM_001297779
Mutation details:
2
records
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10
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2
mutation records.
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NM_022787
Mutation details:
2
records
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2
mutation records.
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