| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014675.4 | 122 | Missense Mutation | ATC,GTC | I26V | NP_055490.4 |
| XM_006711058.3 | 122 | Intron | XP_006711121.1 | ||
| XM_011542468.1 | 122 | Missense Mutation | ATC,GTC | I28V | XP_011540770.1 |
| XM_011542470.2 | 122 | Missense Mutation | ATC,GTC | I28V | XP_011540772.1 |
| XM_017002913.1 | 122 | Missense Mutation | ATC,GTC | I28V | XP_016858402.1 |
| XM_017002914.1 | 122 | Missense Mutation | ATC,GTC | I28V | XP_016858403.1 |
| XM_017002915.1 | 122 | Missense Mutation | ATC,GTC | I28V | XP_016858404.1 |