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 IGF2:
 
NM_000612
Mutation details:
5
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NM_001007139
Mutation details:
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NM_001127598
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Mutation details:
6
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NM_001291861
Mutation details:
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NM_001291862
Mutation details:
5
records
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