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 SH3GL3:
NM_001301108
Mutation details:
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NM_001301109
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Mutation details:
1
records
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1
mutation records.
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NM_003027
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