| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001890.2 | 1369 | Missense Mutation | AGA,AGC | R431S | NP_001001890.1 |
| NM_001122607.1 | 1369 | Intron | NP_001116079.1 | ||
| NM_001754.4 | 1369 | Missense Mutation | AGA,AGC | R458S | NP_001745.2 |
| XM_005261068.3 | 1369 | Missense Mutation | AGA,AGC | R446S | XP_005261125.1 |
| XM_005261069.4 | 1369 | Missense Mutation | AGA,AGC | R394S | XP_005261126.1 |
| XM_011529766.2 | 1369 | Missense Mutation | AGA,AGC | R458S | XP_011528068.1 |
| XM_011529767.2 | 1369 | Missense Mutation | AGA,AGC | R445S | XP_011528069.1 |
| XM_011529768.2 | 1369 | Missense Mutation | AGA,AGC | R381S | XP_011528070.1 |
| XM_011529770.2 | 1369 | Intron | XP_011528072.1 | ||
| XM_017028487.1 | 1369 | Missense Mutation | AGA,AGC | R407S | XP_016883976.1 |