| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308292.1 | 1113 | Intron | NP_001295221.1 | ||
| NM_144727.2 | 1113 | Intron | NP_653328.1 | ||
| XM_005249952.3 | 1113 | Missense Mutation | CGC,TGC | R161C | XP_005250009.1 |
| XM_011515836.1 | 1113 | Missense Mutation | CGC,TGC | R161C | XP_011514138.1 |
| XM_011515837.2 | 1113 | Missense Mutation | CGC,TGC | R126C | XP_011514139.1 |
| XM_017011773.1 | 1113 | Intron | XP_016867262.1 |