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 RBMXL1:
NM_001162536
Mutation details:
17
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NM_019610
Mutation details:
17
records
Showing
1
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10
/
17
mutation records.
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2
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