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 TRMT1:
 
NM_001136035
Mutation details:
20
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NM_001142554
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Mutation details:
20
records
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NM_017722
Mutation details:
20
records
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