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 MYH2:
 
NM_001100112
Mutation details:
63
records
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63
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NM_017534
Mutation details:
63
records
Showing
1
-
10
/
63
mutation records.
Page
1
/
7
First
Prev
Next
Last
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Download Data