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 LARP1B:
 
NM_001278604
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Mutation details:
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NM_018078
Mutation details:
11
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NM_032239
Mutation details:
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NM_178043
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Mutation details:
7
records
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7
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