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 TYMP:
 
NM_001113755
Mutation details:
7
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NM_001113756
Mutation details:
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NM_001257988
Mutation details:
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NM_001257989
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Mutation details:
7
records
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7
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NM_001953
Mutation details:
7
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