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 HEMGN:
NM_018437
Mutation details:
3
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NM_197978
Mutation details:
3
records
Showing
1
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10
/
3
mutation records.
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1
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1
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