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 USP39:
 
NM_001256725
Mutation details:
3
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NM_001256727
Mutation details:
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NM_001256728
No image for this transcript.
Mutation details:
3
records
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1
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10
/
3
mutation records.
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NM_006590
Mutation details:
3
records
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3
mutation records.
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NM_001256726
No image for this transcript.
Mutation details:
2
records
Showing
1
-
10
/
2
mutation records.
Page
1
/
1
First
Prev
Next
Last
Jump to page
Download Data