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 ELN:
 
NM_000501
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NM_001081752
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NM_001081753
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NM_001081754
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NM_001081755
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NM_001278912
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NM_001278913
Mutation details:
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NM_001278914
Mutation details:
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NM_001278915
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Mutation details:
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NM_001278916
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Mutation details:
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NM_001278917
Mutation details:
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NM_001278918
Mutation details:
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NM_001278939
Mutation details:
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