| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001324511.1 | 5182 | Intron | NP_001311440.1 | ||
| NM_001324512.1 | 5182 | Missense Mutation | AGA,GGA | R1498G | NP_001311441.1 |
| NM_030955.3 | 5182 | Missense Mutation | AGA,GGA | R1583G | NP_112217.2 |
| XM_017009905.1 | 5182 | Missense Mutation | AGA,GGA | R1620G | XP_016865394.1 |
| XM_017009906.1 | 5182 | Missense Mutation | AGA,GGA | R1456G | XP_016865395.1 |
| XM_017009907.1 | 5182 | Missense Mutation | AGA,GGA | R1101G | XP_016865396.1 |
| XM_017009908.1 | 5182 | Missense Mutation | AGA,GGA | R982G | XP_016865397.1 |
| XM_017009909.1 | 5182 | Missense Mutation | AGA,GGA | R978G | XP_016865398.1 |