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 SPHK2:
 
NM_001204158
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Mutation details:
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NM_001204159
Mutation details:
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NM_001204160
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Mutation details:
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NM_001243876
Mutation details:
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NM_020126
Mutation details:
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