| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001076552.2 | 198 | Missense Mutation | ACC,CCC | T42P | NP_001070020.2 |
| NM_001242393.1 | 198 | Intron | NP_001229322.1 | ||
| NM_018677.3 | 198 | Missense Mutation | ACC,CCC | T42P | NP_061147.1 |
| XM_005260455.1 | 198 | Missense Mutation | ACC,CCC | T42P | XP_005260512.1 |
| XM_005260456.1 | 198 | Missense Mutation | ACC,CCC | T42P | XP_005260513.1 |
| XM_006723826.1 | 198 | Intron | XP_006723889.1 | ||
| XM_011528905.1 | 198 | Missense Mutation | ACC,CCC | T42P | XP_011527207.1 |
| XM_011528906.1 | 198 | Missense Mutation | ACC,CCC | T42P | XP_011527208.1 |
| XM_011528907.1 | 198 | Missense Mutation | ACC,CCC | T42P | XP_011527209.1 |
| XM_011528908.1 | 198 | Missense Mutation | ACC,CCC | T42P | XP_011527210.1 |
| XM_011528909.2 | 198 | Intron | XP_011527211.1 | ||
| XM_011528911.1 | 198 | Intron | XP_011527213.1 | ||
| XM_011528912.2 | 198 | Intron | XP_011527214.1 |