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 HNRNPR:
 
NM_001102398
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Mutation details:
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NM_001297620
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NM_005826
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NM_001102397
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NM_001102399
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NM_001297621
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NM_001297622
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