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 CHRND:
 
NM_000751
Mutation details:
8
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NM_001256657
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Mutation details:
7
records
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7
mutation records.
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NM_001311195
Mutation details:
4
records
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4
mutation records.
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NM_001311196
No image for this transcript.
Mutation details:
6
records
Showing
1
-
10
/
6
mutation records.
Page
1
/
1
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Next
Last
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Download Data