| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001190971.1 | 369 | Missense Mutation | CAG,CCG | Q52P | NP_001177900.1 |
| NM_004764.4 | 369 | Missense Mutation | CAG,CCG | Q52P | NP_004755.2 |
| XM_011539002.2 | 369 | Missense Mutation | CAG,CCG | Q52P | XP_011537304.1 |
| XM_011539003.2 | 369 | Missense Mutation | CAG,CCG | Q52P | XP_011537305.1 |
| XM_011539004.2 | 369 | Missense Mutation | CAG,CCG | Q52P | XP_011537306.1 |
| XM_011539005.1 | 369 | Missense Mutation | CAG,CCG | Q52P | XP_011537307.1 |
| XM_011539006.2 | 369 | Intron | XP_011537308.1 | ||
| XM_017020229.1 | 369 | Missense Mutation | CAG,CCG | Q52P | XP_016875718.1 |