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 FOXP1:
 
NM_001244808
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Mutation details:
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NM_001244812
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Mutation details:
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NM_001244813
Mutation details:
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NM_001244814
Mutation details:
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NM_001244815
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Mutation details:
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NM_001244816
Mutation details:
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NM_032682
Mutation details:
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NM_001244810
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Mutation details:
5
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