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 ST5:
 
NM_005418
Mutation details:
22
records
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NM_139157
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Mutation details:
13
records
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13
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NM_213618
Mutation details:
22
records
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1
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10
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22
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