| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_024923.3 | 5538 | Missense Mutation | GCC,GTC | A1858V | NP_079199.2 |
| XM_005264994.3 | 5538 | Intron | XP_005265051.1 | ||
| XM_011533538.2 | 5538 | Intron | XP_011531840.1 | ||
| XM_017006018.1 | 5538 | Missense Mutation | GCC,GTC | A986V | XP_016861507.1 |
| XM_017006019.1 | 5538 | Missense Mutation | GCC,GTC | A975V | XP_016861508.1 |
| XM_017006020.1 | 5538 | Missense Mutation | GCC,GTC | A963V | XP_016861509.1 |
| XM_017006021.1 | 5538 | Intron | XP_016861510.1 |