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 MXD1:
 
NM_001202513
Mutation details:
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NM_001202514
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Mutation details:
2
records
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2
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NM_002357
Mutation details:
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