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 SPHKAP:
 
NM_001142644
Mutation details:
42
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NM_030623
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Mutation details:
42
records
Showing
1
-
10
/
42
mutation records.
Page
1
/
5
First
Prev
Next
Last
Jump to page
Download Data