Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001079536.1 | 1047 | Missense Mutation | AGG,ATG | R266M | NP_001073004.1 |
NM_001297668.1 | 1047 | Missense Mutation | AGG,ATG | R198M | NP_001284597.1 |
NM_053017.4 | 1047 | Missense Mutation | AGG,ATG | R266M | NP_443750.2 |
XM_005252779.3 | 1047 | Missense Mutation | AGG,ATG | R266M | XP_005252836.1 |
XM_006718136.3 | 1047 | Missense Mutation | AGG,ATG | R266M | XP_006718199.1 |
XM_011519879.2 | 1047 | Missense Mutation | AGG,ATG | R266M | XP_011518181.1 |
XM_017017171.1 | 1047 | Missense Mutation | AGG,ATG | R74M | XP_016872660.1 |