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 IFT122:
 
NM_001280541
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NM_001280545
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NM_001280546
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NM_018262
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NM_052985
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NM_052989
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NM_052990
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