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 AP4B1:
 
NM_001253852
Mutation details:
5
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NM_001253853
Mutation details:
5
records
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5
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NM_001308312
Mutation details:
4
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NM_006594
Mutation details:
5
records
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10
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5
mutation records.
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