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 NPC1L1:
 
NM_001101648
Mutation details:
20
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NM_001300967
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Mutation details:
13
records
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13
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NM_013389
Mutation details:
20
records
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10
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