| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014939.3 | 4483 | Missense Mutation | GCA,GGA | A1392G | NP_055754.2 |
| XM_005258233.2 | 4483 | Missense Mutation | GCA,GGA | A1393G | XP_005258290.1 |
| XM_005258234.2 | 4483 | Missense Mutation | GCA,GGA | A1363G | XP_005258291.1 |
| XM_005258235.3 | 4483 | Missense Mutation | GCA,GGA | A1118G | XP_005258292.1 |
| XM_006722420.3 | 4483 | Intron | XP_006722483.1 | ||
| XM_011525884.2 | 4483 | UTR 3 | XP_011524186.1 | ||
| XM_017025615.1 | 4483 | Missense Mutation | GCA,GGA | A1367G | XP_016881104.1 |
| XM_017025616.1 | 4483 | Missense Mutation | GCA,GGA | A1362G | XP_016881105.1 |
| XM_017025617.1 | 4483 | UTR 3 | XP_016881106.1 |