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 NFATC2:
 
NM_001136021
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Mutation details:
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NM_001258292
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Mutation details:
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NM_001258294
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Mutation details:
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NM_001258295
Mutation details:
9
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NM_001258296
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Mutation details:
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NM_001258297
Mutation details:
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NM_012340
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NM_173091
Mutation details:
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