| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_019589.2 | 284 | Missense Mutation | TCG,TTG | S39L | NP_062535.2 |
| XM_005267860.3 | 284 | Missense Mutation | TCG,TTG | S39L | XP_005267917.1 |
| XM_011536966.2 | 284 | Intron | XP_011535268.1 | ||
| XM_011536967.1 | 284 | Missense Mutation | TCG,TTG | S39L | XP_011535269.1 |