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 RHOT1:
 
NM_001033566
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NM_001033567
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NM_001033568
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NM_001288754
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NM_001288755
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NM_001288758
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NM_018307
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