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 WRAP53:
 
NM_001143990
Mutation details:
2
records
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10
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2
mutation records.
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NM_001143991
Mutation details:
2
records
Showing
1
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10
/
2
mutation records.
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1
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NM_001143992
Mutation details:
2
records
Showing
1
-
10
/
2
mutation records.
Page
1
/
1
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Last
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NM_018081
Mutation details:
2
records
Showing
1
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10
/
2
mutation records.
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1
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1
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