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 ANKRD50:
 
NM_001167882
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Mutation details:
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NM_020337
Mutation details:
20
records
Showing
1
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10
/
20
mutation records.
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2
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Download Data