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 FTCD:
NM_006657
Mutation details:
11
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NM_206965
Mutation details:
11
records
Showing
1
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10
/
11
mutation records.
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1
/
2
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