| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135862.2 | 1655 | Missense Mutation | ACT,CCT | T460P | NP_001129334.1 |
| NM_001242450.1 | 1655 | Missense Mutation | ACT,CCT | T448P | NP_001229379.1 |
| NM_001284296.1 | 1655 | Missense Mutation | ACT,CCT | T298P | NP_001271225.1 |
| NM_138415.4 | 1655 | Missense Mutation | ACT,CCT | T502P | NP_612424.1 |
| XM_006724122.1 | 1655 | Missense Mutation | ACT,CCT | T460P | XP_006724185.1 |
| XM_011529855.1 | 1655 | Intron | XP_011528157.1 |