| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001267571.1 | 2728 | Missense Mutation | CGC,TGC | R850C | NP_001254500.1 |
| NM_001267572.1 | 2728 | Missense Mutation | CGC,TGC | R390C | NP_001254501.1 |
| NM_018421.3 | 2728 | Missense Mutation | CGC,TGC | R839C | NP_060891.3 |
| XM_011518843.1 | 2728 | Missense Mutation | CGC,TGC | R390C | XP_011517145.1 |
| XM_011518844.2 | 2728 | Intron | XP_011517146.1 | ||
| XM_017014899.1 | 2728 | Missense Mutation | CGC,TGC | R405C | XP_016870388.1 |