| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020310.2 | 877 | Missense Mutation | CGC,GGC | R531G | NP_064706.1 |
| XM_011523868.2 | 877 | Missense Mutation | CGC,GGC | R539G | XP_011522170.1 |
| XM_011523869.1 | 877 | Missense Mutation | CGC,GGC | R250G | XP_011522171.1 |
| XM_017024654.1 | 877 | Missense Mutation | CGC,GGC | R250G | XP_016880143.1 |