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 HECW1:
 
NM_001287059
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Mutation details:
31
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NM_015052
Mutation details:
33
records
Showing
1
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10
/
33
mutation records.
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1
/
4
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Last
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Download Data