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 AP1M2:
 
NM_001300887
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Mutation details:
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NM_005498
Mutation details:
9
records
Showing
1
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10
/
9
mutation records.
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1
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1
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Download Data