| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281301.1 | 462 | Missense Mutation | ATG,GTG | M34V | NP_001268230.1 |
| NM_004856.6 | 462 | Missense Mutation | AAT,AGT | N98S | NP_004847.2 |
| NM_138555.3 | 462 | Missense Mutation | AAT,AGT | N98S | NP_612565.1 |
| XM_005254796.2 | 462 | Missense Mutation | AAT,AGT | N98S | XP_005254853.1 |
| XM_005254797.2 | 462 | Missense Mutation | AAT,AGT | N98S | XP_005254854.1 |
| XM_005254798.2 | 462 | Missense Mutation | AAT,AGT | N98S | XP_005254855.1 |
| XM_005254799.2 | 462 | Missense Mutation | AAT,AGT | N98S | XP_005254856.1 |
| XM_011522238.1 | 462 | Missense Mutation | ATG,GTG | M34V | XP_011520540.1 |
| XM_011522239.2 | 462 | UTR 5 | XP_011520541.1 | ||
| XM_011522240.1 | 462 | Intron | XP_011520542.1 | ||
| XM_017022733.1 | 462 | Missense Mutation | AAT,AGT | N98S | XP_016878222.1 |