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 RAG2:
NM_000536
Mutation details:
10
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NM_001243785
Mutation details:
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NM_001243786
Mutation details:
10
records
Showing
1
-
10
/
10
mutation records.
Page
1
/
1
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Next
Last
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