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 PGM1:
 
NM_001172818
Mutation details:
7
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7
mutation records.
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NM_002633
Mutation details:
9
records
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NM_001172819
Mutation details:
4
records
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10
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4
mutation records.
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