| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001136051.2 | 3451 | Missense Mutation | CTA,GTA | L990V | NP_001129523.1 |
| NM_153377.4 | 3451 | Missense Mutation | CTA,GTA | L1050V | NP_700356.2 |
| XM_011537893.2 | 3451 | Missense Mutation | CTA,GTA | L972V | XP_011536195.1 |
| XM_017018790.1 | 3451 | Intron | XP_016874279.1 |