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 CLINT1:
NM_001195555
Mutation details:
7
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NM_001195556
Mutation details:
7
records
Showing
1
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10
/
7
mutation records.
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1
/
1
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NM_014666
Mutation details:
7
records
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1
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10
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7
mutation records.
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