| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142535.1 | 373 | Missense Mutation | GCA,GGA | A11G | NP_001136007.1 |
| NM_001142536.1 | 373 | Missense Mutation | GCA,GGA | A11G | NP_001136008.1 |
| NM_001142537.1 | 373 | Intron | NP_001136009.1 | ||
| NM_001142538.1 | 373 | Intron | NP_001136010.1 | ||
| NM_033101.3 | 373 | Missense Mutation | GCA,GGA | A11G | NP_149092.2 |
| XM_017018458.1 | 373 | Missense Mutation | GCA,GGA | A11G | XP_016873947.1 |