| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145114.1 | 3827 | Missense Mutation | AGG,GGG | R1169G | NP_001138586.1 |
| NM_001284337.1 | 3827 | Missense Mutation | AGG,GGG | R1130G | NP_001271266.1 |
| NM_015179.3 | 3827 | Missense Mutation | AGG,GGG | R1230G | NP_055994.2 |
| XM_011539555.1 | 3827 | Missense Mutation | AGG,GGG | R1202G | XP_011537857.1 |
| XM_011539556.2 | 3827 | Intron | XP_011537858.1 |