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 RAB23:
 
NM_001278666
Mutation details:
2
records
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mutation records.
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NM_001278667
Mutation details:
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records
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NM_001278668
Mutation details:
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NM_016277
Mutation details:
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NM_183227
Mutation details:
2
records
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2
mutation records.
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