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 SKIL:
 
NM_001145097
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Mutation details:
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NM_001145098
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Mutation details:
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NM_001248008
Mutation details:
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NM_005414
Mutation details:
16
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