| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032172.2 | 139 | Missense Mutation | GCA,GGA | A25G | NP_115548.1 |
| XM_005249883.4 | 139 | Missense Mutation | GCA,GGA | A25G | XP_005249940.1 |
| XM_006715790.1 | 139 | Missense Mutation | GCA,GGA | A25G | XP_006715853.1 |
| XM_006715791.2 | 139 | Missense Mutation | GCA,GGA | A25G | XP_006715854.1 |
| XM_011515573.1 | 139 | Missense Mutation | GCA,GGA | A25G | XP_011513875.1 |
| XM_011515574.1 | 139 | UTR 5 | XP_011513876.1 | ||
| XM_011515577.1 | 139 | Intron | XP_011513879.1 | ||
| XM_011515578.1 | 139 | UTR 5 | XP_011513880.1 |