| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001190482.1 | 569 | Missense Mutation | AGA,GGA | R11G | NP_001177411.1 |
| NM_006200.5 | 569 | Missense Mutation | AGA,GGA | R11G | NP_006191.2 |
| XM_005252039.3 | 569 | Missense Mutation | AGA,GGA | R11G | XP_005252096.1 |
| XM_011518769.2 | 569 | Missense Mutation | AGA,GGA | R11G | XP_011517071.1 |
| XM_011518770.2 | 569 | Intron | XP_011517072.1 | ||
| XM_017014800.1 | 569 | Intron | XP_016870289.1 |