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 NBR1:
 
NM_001291571
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Mutation details:
14
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NM_001291572
Mutation details:
14
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14
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NM_005899
Mutation details:
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NM_031862
Mutation details:
15
records
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