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 RALYL:
 
NM_001100391
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Mutation details:
14
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NM_001100392
Mutation details:
14
records
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mutation records.
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NM_001100393
Mutation details:
14
records
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14
mutation records.
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NM_001287243
Mutation details:
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NM_173848
Mutation details:
14
records
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14
mutation records.
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NM_001287244
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Mutation details:
11
records
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1
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10
/
11
mutation records.
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2
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