| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001167749.2 | 6198 | Missense Mutation | ACG,ATG | T1421M | NP_001161221.1 |
| NM_001297772.1 | 6198 | Missense Mutation | ACG,ATG | T1482M | NP_001284701.1 |
| NM_018417.5 | 6198 | Missense Mutation | ACG,ATG | T1574M | NP_060887.2 |
| XM_005245330.4 | 6198 | Intron | XP_005245387.1 | ||
| XM_006711449.3 | 6198 | Missense Mutation | ACG,ATG | T1511M | XP_006711512.1 |
| XM_011509760.2 | 6198 | Missense Mutation | ACG,ATG | T1574M | XP_011508062.1 |
| XM_011509762.2 | 6198 | Missense Mutation | ACG,ATG | T1526M | XP_011508064.1 |
| XM_011509763.2 | 6198 | Missense Mutation | ACG,ATG | T1520M | XP_011508065.1 |
| XM_011509766.2 | 6198 | Intron | XP_011508068.1 | ||
| XM_017001778.1 | 6198 | Intron | XP_016857267.1 |