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 PLEKHG6:
 
NM_001144856
Mutation details:
19
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NM_001144857
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Mutation details:
19
records
Showing
1
-
10
/
19
mutation records.
Page
1
/
2
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Last
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NM_018173
Mutation details:
19
records
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1
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10
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19
mutation records.
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