| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300912.1 | 348 | Nonsense Mutation | CGA,TGA | R66* | NP_001287841.1 |
| NM_032433.2 | 348 | Nonsense Mutation | CGA,TGA | R66* | NP_115809.1 |
| XM_005260098.3 | 348 | UTR 5 | XP_005260155.1 | ||
| XM_006722924.2 | 348 | Nonsense Mutation | CGA,TGA | R66* | XP_006722987.1 |
| XM_011528362.2 | 348 | Nonsense Mutation | CGA,TGA | R66* | XP_011526664.1 |
| XM_011528363.2 | 348 | UTR 5 | XP_011526665.1 | ||
| XM_011528365.2 | 348 | UTR 5 | XP_011526667.1 | ||
| XM_011528366.2 | 348 | UTR 5 | XP_011526668.1 | ||
| XM_011528367.2 | 348 | UTR 5 | XP_011526669.1 | ||
| XM_011528368.2 | 348 | UTR 5 | XP_011526670.1 | ||
| XM_011528369.2 | 348 | UTR 5 | XP_011526671.1 | ||
| XM_011528371.2 | 348 | Intron | XP_011526673.1 | ||
| XM_011528372.2 | 348 | Intron | XP_011526674.1 | ||
| XM_017027367.1 | 348 | Nonsense Mutation | CGA,TGA | R66* | XP_016882856.1 |
| XM_017027368.1 | 348 | UTR 5 | XP_016882857.1 | ||
| XM_017027369.1 | 348 | UTR 5 | XP_016882858.1 | ||
| XM_017027370.1 | 348 | UTR 5 | XP_016882859.1 | ||
| XM_017027371.1 | 348 | UTR 5 | XP_016882860.1 |