| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242466.1 | 1640 | Intron | NP_001229395.1 | ||
| NM_181504.3 | 1640 | Intron | NP_852556.2 | ||
| NM_181523.2 | 1640 | Missense Mutation | CGG,TGG | R90W | NP_852664.1 |
| NM_181524.1 | 1640 | Intron | NP_852665.1 | ||
| XM_005248542.3 | 1640 | Missense Mutation | CGG,TGG | R90W | XP_005248599.1 |
| XM_011543493.2 | 1640 | Intron | XP_011541795.1 | ||
| XM_017009585.1 | 1640 | Missense Mutation | CGG,TGG | R90W | XP_016865074.1 |
| XM_017009586.1 | 1640 | Intron | XP_016865075.1 |