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 WNK1:
 
NM_001184985
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Mutation details:
25
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NM_014823
Mutation details:
21
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NM_018979
Mutation details:
24
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NM_213655
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Mutation details:
27
records
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27
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