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 PTPRN2:
 
NM_001308267
Mutation details:
31
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NM_001308268
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Mutation details:
32
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NM_002847
Mutation details:
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NM_130842
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Mutation details:
30
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NM_130843
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Mutation details:
30
records
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30
mutation records.
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3
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