| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012335.3 | 3059 | Missense Mutation | CAT,CGT | H998R | NP_036467.2 |
| XM_011528024.1 | 3059 | Missense Mutation | CAT,CGT | H1019R | XP_011526326.1 |
| XM_011528025.1 | 3059 | Missense Mutation | CAT,CGT | H1015R | XP_011526327.1 |
| XM_011528026.1 | 3059 | Missense Mutation | CAT,CGT | H990R | XP_011526328.1 |
| XM_011528027.1 | 3059 | Missense Mutation | CAT,CGT | H974R | XP_011526329.1 |
| XM_011528028.2 | 3059 | Intron | XP_011526330.1 | ||
| XM_017026821.1 | 3059 | Missense Mutation | CAT,CGT | H994R | XP_016882310.1 |