| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_182489.1 | 818 | Missense Mutation | CGC,TGC | R60C | NP_872295.1 |
| XM_011516137.2 | 818 | Missense Mutation | CGC,TGC | R38C | XP_011514439.1 |
| XM_011516138.2 | 818 | Missense Mutation | CGC,TGC | R38C | XP_011514440.1 |
| XM_011516139.2 | 818 | Missense Mutation | CGC,TGC | R38C | XP_011514441.1 |
| XM_017012150.1 | 818 | Missense Mutation | CGC,TGC | R38C | XP_016867639.1 |