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 HNRNPD:
 
NM_001003810
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Mutation details:
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NM_002138
Mutation details:
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NM_031369
Mutation details:
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NM_031370
Mutation details:
6
records
Showing
1
-
10
/
6
mutation records.
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1
/
1
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Last
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Download Data