Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303127.1 | 774 | Missense Mutation | CGT,TGT | R140C | NP_001290056.1 |
NM_001303128.1 | 774 | Silent Mutation | TCC,TCT | S52S | NP_001290057.1 |
NM_173650.2 | 774 | Missense Mutation | CGT,TGT | R140C | NP_775921.1 |
XM_006711995.3 | 774 | Missense Mutation | CGT,TGT | R140C | XP_006712058.1 |
XM_017003872.1 | 774 | Missense Mutation | CGT,TGT | R140C | XP_016859361.1 |
XM_017003873.1 | 774 | Missense Mutation | CGT,TGT | R140C | XP_016859362.1 |
XM_017003874.1 | 774 | Missense Mutation | CGT,TGT | R140C | XP_016859363.1 |