| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001258008.1 | 2399 | Intron | NP_001244937.1 | ||
| NM_017984.4 | 2399 | Missense Mutation | AGG,GGG | R529G | NP_060454.3 |
| XM_005250479.2 | 2399 | Intron | XP_005250536.1 | ||
| XM_005250480.2 | 2399 | Intron | XP_005250537.1 | ||
| XM_006716035.3 | 2399 | Missense Mutation | AGG,GGG | R531G | XP_006716098.1 |
| XM_006716036.2 | 2399 | Missense Mutation | AGG,GGG | R531G | XP_006716099.1 |
| XM_006716037.3 | 2399 | Missense Mutation | AGG,GGG | R530G | XP_006716100.1 |
| XM_006716038.3 | 2399 | Missense Mutation | AGG,GGG | R530G | XP_006716101.1 |
| XM_006716040.3 | 2399 | Missense Mutation | AGG,GGG | R504G | XP_006716103.1 |
| XM_017012379.1 | 2399 | Intron | XP_016867868.1 | ||
| XM_017012380.1 | 2399 | Intron | XP_016867869.1 |