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 MAPT:
 
NM_001123066
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Mutation details:
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NM_016835
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NM_001123067
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NM_001203251
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NM_001203252
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NM_005910
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NM_016834
Mutation details:
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NM_016841
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Mutation details:
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mutation records.
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