| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012384.4 | 1222 | Missense Mutation | GGC,GTC | G456V | NP_036516.1 |
| XM_005260202.4 | 1222 | Missense Mutation | GGC,GTC | G456V | XP_005260259.1 |
| XM_006723776.2 | 1222 | Missense Mutation | GGC,GTC | G378V | XP_006723839.1 |
| XM_011528779.2 | 1222 | Missense Mutation | GGC,GTC | G378V | XP_011527081.1 |