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 PMEPA1:
 
NM_001255976
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Mutation details:
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NM_020182
Mutation details:
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NM_199169
Mutation details:
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NM_199170
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Mutation details:
5
records
Showing
1
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10
/
5
mutation records.
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1
/
1
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NM_199171
No image for this transcript.
Mutation details:
5
records
Showing
1
-
10
/
5
mutation records.
Page
1
/
1
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Next
Last
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Download Data