| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318756.1 | 332 | Intron | NP_001305685.1 | ||
| NM_178452.5 | 332 | Missense Mutation | ATG,GTG | M51V | NP_848547.4 |
| XM_006721129.2 | 332 | Missense Mutation | ATG,GTG | M51V | XP_006721192.1 |
| XM_011522853.2 | 332 | Missense Mutation | ATG,GTG | M51V | XP_011521155.1 |
| XM_011522854.2 | 332 | Missense Mutation | ATG,GTG | M51V | XP_011521156.1 |
| XM_011522855.2 | 332 | Missense Mutation | ATG,GTG | M51V | XP_011521157.1 |
| XM_011522857.2 | 332 | Missense Mutation | ATG,GTG | M51V | XP_011521159.1 |
| XM_011522858.2 | 332 | Missense Mutation | ATG,GTG | M51V | XP_011521160.1 |
| XM_017022918.1 | 332 | Missense Mutation | ATG,GTG | M51V | XP_016878407.1 |
| XM_017022919.1 | 332 | UTR 5 | XP_016878408.1 | ||
| XM_017022920.1 | 332 | Intron | XP_016878409.1 | ||
| XM_017022921.1 | 332 | Intron | XP_016878410.1 | ||
| XM_017022922.1 | 332 | Intron | XP_016878411.1 |