| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000164.3 | 451 | Missense Mutation | GTC,TTC | V99F | NP_000155.1 |
| NM_001308418.1 | 451 | Missense Mutation | GTC,TTC | V63F | NP_001295347.1 |
| XM_011526709.2 | 451 | Missense Mutation | GTC,TTC | V99F | XP_011525011.1 |
| XM_011526710.2 | 451 | Missense Mutation | GTC,TTC | V99F | XP_011525012.1 |
| XM_011526711.2 | 451 | Missense Mutation | GTC,TTC | V63F | XP_011525013.1 |
| XM_011526713.2 | 451 | Missense Mutation | GTC,TTC | V99F | XP_011525015.1 |
| XM_011526714.2 | 451 | UTR 5 | XP_011525016.1 | ||
| XM_011526715.2 | 451 | UTR 5 | XP_011525017.1 | ||
| XM_011526716.2 | 451 | Missense Mutation | GTC,TTC | V99F | XP_011525018.1 |
| XM_017026584.1 | 451 | Intron | XP_016882073.1 | ||
| XM_017026585.1 | 451 | Intron | XP_016882074.1 | ||
| XM_017026586.1 | 451 | Intron | XP_016882075.1 | ||
| XM_017026587.1 | 451 | Intron | XP_016882076.1 |