| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001032287.2 | 1656 | Intron | NP_001027458.1 | ||
| NM_001127362.1 | 1656 | Missense Mutation | AAG,AGG | K467R | NP_001120834.1 |
| NM_003297.3 | 1656 | Intron | NP_003288.2 | ||
| XM_005269133.2 | 1656 | Intron | XP_005269190.1 | ||
| XM_006719584.2 | 1656 | Intron | XP_006719647.1 | ||
| XM_006719585.2 | 1656 | Intron | XP_006719648.1 | ||
| XM_011538716.2 | 1656 | Intron | XP_011537018.1 | ||
| XM_011538717.2 | 1656 | Intron | XP_011537019.1 |