| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001159488.1 | 1577 | Silent Mutation | AGA,AGG | R436R | NP_001152960.1 |
| NM_030764.3 | 1577 | Missense Mutation | AAC,GAC | N497D | NP_110391.2 |
| XM_006711535.3 | 1577 | Intron | XP_006711598.1 | ||
| XM_011509974.2 | 1577 | Silent Mutation | AGA,AGG | R505R | XP_011508276.1 |
| XM_011509975.2 | 1577 | Silent Mutation | AGA,AGG | R483R | XP_011508277.1 |
| XM_011509976.2 | 1577 | Missense Mutation | AAC,GAC | N475D | XP_011508278.1 |
| XM_017002316.1 | 1577 | Missense Mutation | GAA,GGA | E487G | XP_016857805.1 |
| XM_017002317.1 | 1577 | Missense Mutation | GAA,GGA | E421G | XP_016857806.1 |
| XM_017002318.1 | 1577 | Missense Mutation | GAA,GGA | E394G | XP_016857807.1 |
| XM_017002319.1 | 1577 | Missense Mutation | GAA,GGA | E392G | XP_016857808.1 |