| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005929.5 | 2283 | Missense Mutation | CTG,GTG | L698V | NP_005920.2 |
| NM_033316.3 | 2283 | Intron | NP_201573.1 | ||
| XM_006713643.3 | 2283 | Missense Mutation | CTG,GTG | L724V | XP_006713706.2 |
| XM_011512850.2 | 2283 | Missense Mutation | CTG,GTG | L725V | XP_011511152.1 |
| XM_011512851.2 | 2283 | Intron | XP_011511153.1 |