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 FGL1:
NM_004467
Mutation details:
4
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NM_147203
Mutation details:
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NM_201552
Mutation details:
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NM_201553
Mutation details:
4
records
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1
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10
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4
mutation records.
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1
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