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 GRAMD1C:
 
NM_001172105
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Mutation details:
8
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NM_017577
Mutation details:
11
records
Showing
1
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10
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11
mutation records.
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2
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