| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001029939.3 | 3988 | Missense Mutation | AGG,GGG | R1203G | NP_001025110.2 |
| NM_001167583.2 | 3988 | Missense Mutation | AGG,GGG | R1203G | NP_001161055.1 |
| NM_001174157.1 | 3988 | Missense Mutation | AGG,GGG | R1153G | NP_001167628.1 |
| NM_001174158.1 | 3988 | Missense Mutation | AGG,GGG | R1117G | NP_001167629.1 |
| NM_001289394.1 | 3988 | Missense Mutation | AGG,GGG | R1203G | NP_001276323.1 |
| NM_020863.3 | 3988 | Missense Mutation | AGG,GGG | R1215G | NP_065914.2 |
| XM_011517203.1 | 3988 | Missense Mutation | AGG,GGG | R1203G | XP_011515505.1 |
| XM_011517204.2 | 3988 | Missense Mutation | AGG,GGG | R1153G | XP_011515506.1 |
| XM_011517206.1 | 3988 | Intron | XP_011515508.1 | ||
| XM_017013716.1 | 3988 | Intron | XP_016869205.1 |