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 PTBP2:
 
NM_001300985
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Mutation details:
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NM_001300986
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NM_001300987
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NM_001300988
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NM_001300989
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NM_001300990
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NM_021190
Mutation details:
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