Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001290056.1 | 898 | Intron | NP_001276985.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152658.2 | 898 | Missense Mutation | CGC,TGC | R182C | NP_689871.1 |
XM_005258623.2 | 898 | Missense Mutation | CGC,TGC | R139C | XP_005258680.1 |
XM_011526604.2 | 898 | Missense Mutation | CGC,TGC | R139C | XP_011524906.1 |