| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001276495.1 | 306 | Missense Mutation | TCA,TTA | S23L | NP_001263424.1 |
| NM_001316339.1 | 306 | Intron | NP_001303268.1 | ||
| NM_002780.4 | 306 | Missense Mutation | TCA,TTA | S23L | NP_002771.2 |
| NM_213633.2 | 306 | Missense Mutation | TCA,TTA | S23L | NP_998798.1 |
| XM_017026995.1 | 306 | Intron | XP_016882484.1 | ||
| XM_017026996.1 | 306 | Missense Mutation | TCA,TTA | S39L | XP_016882485.1 |
| XM_017026997.1 | 306 | Missense Mutation | TCA,TTA | S23L | XP_016882486.1 |
| XM_017026998.1 | 306 | Intron | XP_016882487.1 | ||
| XM_017026999.1 | 306 | Intron | XP_016882488.1 | ||
| XM_017027000.1 | 306 | Missense Mutation | TCA,TTA | S39L | XP_016882489.1 |
| XM_017027001.1 | 306 | Intron | XP_016882490.1 | ||
| XM_017027002.1 | 306 | Intron | XP_016882491.1 |