| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199633.1 | 2059 | Missense Mutation | GTG,TTG | V670L | NP_001186562.1 |
| NM_022127.2 | 2059 | Missense Mutation | GTG,TTG | V670L | NP_071410.1 |
| XM_011518905.2 | 2059 | Missense Mutation | GTG,TTG | V698L | XP_011517207.1 |
| XM_011518906.2 | 2059 | Missense Mutation | GTG,TTG | V698L | XP_011517208.1 |
| XM_011518907.2 | 2059 | Missense Mutation | GTG,TTG | V587L | XP_011517209.1 |
| XM_011518908.2 | 2059 | Missense Mutation | GTG,TTG | V457L | XP_011517210.1 |
| XM_011518909.2 | 2059 | Intron | XP_011517211.1 | ||
| XM_011518910.2 | 2059 | Intron | XP_011517212.1 |