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 NCR1:
 
NM_001145457
Mutation details:
9
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NM_001145458
Mutation details:
9
records
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1
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10
/
9
mutation records.
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1
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NM_004829
Mutation details:
9
records
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NM_001242356
No image for this transcript.
Mutation details:
5
records
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1
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10
/
5
mutation records.
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NM_001242357
No image for this transcript.
Mutation details:
5
records
Showing
1
-
10
/
5
mutation records.
Page
1
/
1
First
Prev
Next
Last
Jump to page
Download Data