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 APLP2:
 
NM_001142276
Mutation details:
19
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NM_001142277
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Mutation details:
18
records
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18
mutation records.
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NM_001142278
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Mutation details:
14
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NM_001243299
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Mutation details:
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NM_001642
Mutation details:
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