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 GPR132:
 
NM_001278694
Mutation details:
4
records
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mutation records.
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NM_001278695
No image for this transcript.
Mutation details:
4
records
Showing
1
-
10
/
4
mutation records.
Page
1
/
1
First
Prev
Next
Last
Jump to page
Download Data
NM_001278696
No image for this transcript.
Mutation details:
3
records
Showing
1
-
10
/
3
mutation records.
Page
1
/
1
First
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Next
Last
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NM_013345
Mutation details:
4
records
Showing
1
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10
/
4
mutation records.
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1
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1
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