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 PTK2B:
 
NM_004103
Mutation details:
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NM_173174
Mutation details:
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NM_173176
Mutation details:
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NM_173175
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Mutation details:
9
records
Showing
1
-
10
/
9
mutation records.
Page
1
/
1
First
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Next
Last
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Download Data