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 MELK:
 
NM_001256685
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NM_001256687
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NM_001256688
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NM_001256689
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NM_001256690
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Mutation details:
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NM_001256691
Mutation details:
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NM_001256692
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NM_001256693
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NM_014791
Mutation details:
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