| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001173984.2 | 2158 | Intron | NP_001167455.1 | ||
| NM_013263.4 | 2158 | Intron | NP_037395.2 | ||
| XM_011523046.2 | 2158 | Intron | XP_011521348.1 | ||
| XM_011523047.2 | 2158 | Missense Mutation | CCT,TCT | P655S | XP_011521349.1 |
| XM_011523048.2 | 2158 | Intron | XP_011521350.1 | ||
| XM_011523049.2 | 2158 | Intron | XP_011521351.1 | ||
| XM_011523050.2 | 2158 | Missense Mutation | CCT,TCT | P437S | XP_011521352.1 |
| XM_017023179.1 | 2158 | Intron | XP_016878668.1 | ||
| XM_017023180.1 | 2158 | Intron | XP_016878669.1 | ||
| XM_017023181.1 | 2158 | Missense Mutation | CCT,TCT | P436S | XP_016878670.1 |