| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009998.3 | 710 | Intron | NP_001009998.1 | ||
| NM_032627.4 | 710 | Intron | NP_116016.1 | ||
| XM_005259790.3 | 710 | Missense Mutation | GTC,TTC | V143F | XP_005259847.1 |
| XM_006722665.3 | 710 | Missense Mutation | GTC,TTC | V143F | XP_006722728.1 |
| XM_006722666.2 | 710 | Intron | XP_006722729.1 | ||
| XM_006722668.2 | 710 | Intron | XP_006722731.1 | ||
| XM_017026431.1 | 710 | Missense Mutation | GTC,TTC | V143F | XP_016881920.1 |
| XM_017026432.1 | 710 | Missense Mutation | GTC,TTC | V132F | XP_016881921.1 |
| XM_017026433.1 | 710 | Intron | XP_016881922.1 | ||
| XM_017026434.1 | 710 | Missense Mutation | GTC,TTC | V143F | XP_016881923.1 |
| XM_017026435.1 | 710 | Missense Mutation | GTC,TTC | V132F | XP_016881924.1 |
| XM_017026436.1 | 710 | Intron | XP_016881925.1 | ||
| XM_017026437.1 | 710 | Missense Mutation | GTC,TTC | V143F | XP_016881926.1 |