| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001134477.2 | 1937 | Missense Mutation | TCG,TTG | S564L | NP_001127949.1 |
| NM_001242992.1 | 1937 | Missense Mutation | TCG,TTG | S579L | NP_001229921.1 |
| NM_002582.3 | 1937 | Missense Mutation | TCG,TTG | S625L | NP_002573.1 |
| XM_011522510.2 | 1937 | Intron | XP_011520812.1 | ||
| XM_011522511.2 | 1937 | Intron | XP_011520813.1 | ||
| XM_011522513.2 | 1937 | Intron | XP_011520815.1 | ||
| XM_011522514.1 | 1937 | Intron | XP_011520816.1 | ||
| XM_017023258.1 | 1937 | Intron | XP_016878747.1 | ||
| XM_017023259.1 | 1937 | Intron | XP_016878748.1 | ||
| XM_017023260.1 | 1937 | Intron | XP_016878749.1 |