| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002772.2 | 3100 | Missense Mutation | AGG,GGG | R969G | NP_002763.2 |
| XM_011529654.1 | 3100 | Missense Mutation | AGG,GGG | R1014G | XP_011527956.1 |
| XM_011529655.1 | 3100 | Missense Mutation | AGG,GGG | R1014G | XP_011527957.1 |
| XM_011529656.2 | 3100 | Missense Mutation | AGG,GGG | R1014G | XP_011527958.1 |
| XM_011529657.1 | 3100 | Missense Mutation | AGG,GGG | R999G | XP_011527959.1 |
| XM_011529658.1 | 3100 | Missense Mutation | AGG,GGG | R987G | XP_011527960.1 |
| XM_011529659.1 | 3100 | Missense Mutation | AGG,GGG | R984G | XP_011527961.1 |