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 PRDX1:
 
NM_001202431
Mutation details:
2
records
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NM_002574
Mutation details:
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NM_181696
Mutation details:
2
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NM_181697
Mutation details:
2
records
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1
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2
mutation records.
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