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 PCMT1:
 
NM_001252049
Mutation details:
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NM_001252050
Mutation details:
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NM_001252051
Mutation details:
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NM_001252052
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Mutation details:
2
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NM_001252053
Mutation details:
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records
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NM_005389
Mutation details:
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