| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001012644.2 | 1067 | Intron | NP_001012662.1 | ||
| NM_001320478.1 | 1067 | Intron | NP_001307407.1 | ||
| NM_001320479.1 | 1067 | Missense Mutation | CGC,CTC | R295L | NP_001307408.1 |
| NM_080611.4 | 1067 | Intron | NP_542178.2 | ||
| NM_177991.2 | 1067 | Intron | NP_817130.1 | ||
| XM_017027654.1 | 1067 | Missense Mutation | CGC,CTC | R335L | XP_016883143.1 |
| XM_017027655.1 | 1067 | Missense Mutation | CGC,CTC | R332L | XP_016883144.1 |
| XM_017027656.1 | 1067 | Intron | XP_016883145.1 | ||
| XM_017027657.1 | 1067 | Missense Mutation | CGC,CTC | R298L | XP_016883146.1 |
| XM_017027658.1 | 1067 | Missense Mutation | CGC,CTC | R232L | XP_016883147.1 |
| XM_017027659.1 | 1067 | Missense Mutation | CGC,CTC | R232L | XP_016883148.1 |
| XM_017027660.1 | 1067 | Missense Mutation | CGC,CTC | R232L | XP_016883149.1 |
| XM_017027661.1 | 1067 | Missense Mutation | CGC,CTC | R232L | XP_016883150.1 |
| XM_017027662.1 | 1067 | Missense Mutation | CGC,CTC | R232L | XP_016883151.1 |