| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010919.2 | 437 | Missense Mutation | GGC,GTC | G12V | NP_001010919.1 |
| NM_001276460.1 | 437 | Intron | NP_001263389.1 | ||
| XM_005266999.3 | 437 | Missense Mutation | GGC,GTC | G12V | XP_005267056.1 |
| XM_011535845.2 | 437 | Missense Mutation | GGC,GTC | G12V | XP_011534147.1 |