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 PTPRS:
 
NM_002850
Mutation details:
38
records
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mutation records.
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NM_130853
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Mutation details:
29
records
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10
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29
mutation records.
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NM_130854
No image for this transcript.
Mutation details:
36
records
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1
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10
/
36
mutation records.
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1
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4
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NM_130855
Mutation details:
29
records
Showing
1
-
10
/
29
mutation records.
Page
1
/
3
First
Prev
Next
Last
Jump to page
Download Data