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 GRM5:
 
NM_000842
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Mutation details:
17
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NM_001143831
Mutation details:
17
records
Showing
1
-
10
/
17
mutation records.
Page
1
/
2
First
Prev
Next
Last
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Download Data