| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_153634.2 | 1655 | Missense Mutation | CAA,CGA | Q542R | NP_705898.1 |
| XM_011537951.2 | 1655 | Intron | XP_011536253.1 | ||
| XM_011537952.2 | 1655 | Intron | XP_011536254.1 | ||
| XM_017018851.1 | 1655 | Missense Mutation | CAA,CGA | Q542R | XP_016874340.1 |
| XM_017018852.1 | 1655 | Missense Mutation | CAA,CGA | Q381R | XP_016874341.1 |