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 TNIP1:
 
NM_001252385
Mutation details:
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NM_001252386
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NM_001252390
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NM_001252391
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NM_001252392
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NM_001252393
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NM_001258454
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NM_001258455
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NM_001258456
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Mutation details:
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NM_006058
Mutation details:
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