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 HCK:
 
NM_001172129
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Mutation details:
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NM_001172130
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Mutation details:
11
records
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10
/
11
mutation records.
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2
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NM_001172131
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Mutation details:
11
records
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10
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11
mutation records.
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NM_001172132
Mutation details:
11
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mutation records.
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NM_001172133
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Mutation details:
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NM_002110
Mutation details:
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