| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001206794.1 | 3824 | Missense Mutation | TCG,TTG | S1222L | NP_001193723.1 |
| NM_016374.5 | 3824 | Missense Mutation | TCG,TTG | S1222L | NP_057458.4 |
| NM_031371.3 | 3824 | Missense Mutation | TCG,TTG | S1136L | NP_112739.2 |
| XM_006711781.2 | 3824 | Missense Mutation | TCG,TTG | S1186L | XP_006711844.1 |
| XM_011544212.2 | 3824 | Missense Mutation | TCG,TTG | S1222L | XP_011542514.1 |
| XM_017001468.1 | 3824 | Missense Mutation | TCG,TTG | S1224L | XP_016856957.1 |
| XM_017001469.1 | 3824 | Missense Mutation | TCG,TTG | S1188L | XP_016856958.1 |
| XM_017001470.1 | 3824 | Missense Mutation | TCG,TTG | S1138L | XP_016856959.1 |
| XM_017001471.1 | 3824 | Intron | XP_016856960.1 | ||
| XM_017001472.1 | 3824 | Missense Mutation | TCG,TTG | S929L | XP_016856961.1 |