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 ASGR2:
 
NM_001181
Mutation details:
5
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NM_001201352
Mutation details:
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NM_080912
Mutation details:
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NM_080913
No image for this transcript.
Mutation details:
5
records
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5
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NM_080914
No image for this transcript.
Mutation details:
5
records
Showing
1
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10
/
5
mutation records.
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1
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1
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