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 SLC18A1:
 
NM_001135691
Mutation details:
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NM_001142324
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Mutation details:
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NM_001142325
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Mutation details:
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NM_003053
Mutation details:
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