| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014611.2 | 16701 | Missense Mutation | CAA,CGA | Q5570R | NP_055426.1 |
| XM_005248700.3 | 16701 | Missense Mutation | CAA,CGA | Q3565R | XP_005248757.1 |
| XM_006715405.3 | 16701 | Missense Mutation | CAA,CGA | Q3718R | XP_006715468.1 |
| XM_011535635.2 | 16701 | Missense Mutation | CAA,CGA | Q5473R | XP_011533937.1 |
| XM_011535636.2 | 16701 | Intron | XP_011533938.1 |