| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001264573.1 | 2654 | UTR 3 | NP_001251503.1 | ||
| NM_001265577.1 | 2654 | Missense Mutation | CGG,GGG | R829G | NP_001252506.1 |
| XM_011524385.2 | 2654 | Missense Mutation | CGG,GGG | R850G | XP_011522687.1 |
| XM_011524386.2 | 2654 | Missense Mutation | CGG,GGG | R841G | XP_011522688.1 |
| XM_011524387.2 | 2654 | Missense Mutation | CGG,GGG | R841G | XP_011522689.1 |
| XM_011524388.2 | 2654 | Missense Mutation | CGG,GGG | R838G | XP_011522690.1 |
| XM_011524389.2 | 2654 | UTR 3 | XP_011522691.1 | ||
| XM_011524390.2 | 2654 | Missense Mutation | CGG,GGG | R815G | XP_011522692.1 |
| XM_011524391.2 | 2654 | Intron | XP_011522693.1 |