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 GRIN2A:
 
NM_000833
Mutation details:
41
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NM_001134407
Mutation details:
41
records
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NM_001134408
No image for this transcript.
Mutation details:
39
records
Showing
1
-
10
/
39
mutation records.
Page
1
/
4
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Next
Last
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Download Data