| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001288732.1 | 3357 | Missense Mutation | TCA,TTA | S1071L | NP_001275661.1 |
| NM_001288733.1 | 3357 | Missense Mutation | TCA,TTA | S1071L | NP_001275662.1 |
| NM_018469.4 | 3357 | Missense Mutation | TCA,TTA | S1078L | NP_060939.3 |
| XM_011524998.1 | 3357 | Missense Mutation | TCA,TTA | S1078L | XP_011523300.1 |
| XM_011524999.1 | 3357 | Missense Mutation | TCA,TTA | S1078L | XP_011523301.1 |
| XM_011525000.1 | 3357 | Missense Mutation | TCA,TTA | S1076L | XP_011523302.1 |
| XM_017024846.1 | 3357 | Missense Mutation | TCA,TTA | S1069L | XP_016880335.1 |
| XM_017024847.1 | 3357 | Intron | XP_016880336.1 |