| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014299.2 | 4116 | Intron | NP_055114.1 | ||
| NM_058243.2 | 4116 | Missense Mutation | CAA,CAT | Q1298H | NP_490597.1 |
| XM_011527854.1 | 4116 | Missense Mutation | CAA,CAT | Q1298H | XP_011526156.1 |
| XM_011527855.1 | 4116 | Intron | XP_011526157.1 | ||
| XM_011527856.2 | 4116 | Intron | XP_011526158.1 |