| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130107.1 | 1191 | Intron | NP_001123579.1 | ||
| NM_005552.4 | 1191 | Intron | NP_005543.2 | ||
| NM_182923.3 | 1191 | Intron | NP_891553.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001100118.1 | 1191 | Missense Mutation | AGG,GGG | R271G | NP_001093588.1 |
| NM_001100119.1 | 1191 | Missense Mutation | AGG,GGG | R271G | NP_001093589.1 |
| NM_005432.3 | 1191 | Missense Mutation | AGG,GGG | R271G | NP_005423.1 |
| XM_005268046.2 | 1191 | Missense Mutation | AGG,GGG | R271G | XP_005268103.1 |
| XM_011537138.2 | 1191 | Missense Mutation | AGG,GGG | R271G | XP_011535440.1 |