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 RAPGEF4:
 
NM_001100397
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NM_001282899
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NM_001282900
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NM_001282901
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NM_007023
Mutation details:
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