Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001127219.1 | 729 | Missense Mutation | CGT,TGT | R48C | NP_001120691.1 |
NM_032592.3 | 729 | Missense Mutation | CGT,TGT | R48C | NP_115981.1 |
XM_005253170.3 | 729 | Missense Mutation | CGT,TGT | R149C | XP_005253227.2 |
XM_005253172.2 | 729 | Intron | XP_005253229.1 | ||
XM_006718348.2 | 729 | Intron | XP_006718411.1 | ||
XM_011520406.2 | 729 | Missense Mutation | CGT,TGT | R149C | XP_011518708.1 |
XM_011520407.1 | 729 | Intron | XP_011518709.1 | ||
XM_011520410.2 | 729 | UTR 5 | XP_011518712.1 | ||
XM_017018421.1 | 729 | Missense Mutation | CGT,TGT | R149C | XP_016873910.1 |