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 PXK:
 
NM_001289095
Mutation details:
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NM_001289096
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Mutation details:
4
records
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10
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4
mutation records.
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NM_001289098
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Mutation details:
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NM_001289099
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Mutation details:
4
records
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4
mutation records.
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NM_001289100
Mutation details:
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NM_001289101
Mutation details:
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NM_017771
Mutation details:
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