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 PEX1:
 
NM_000466
Mutation details:
14
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NM_001282678
Mutation details:
13
records
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NM_001282677
Mutation details:
11
records
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10
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11
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