| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002000.3 | 555 | Missense Mutation | CGG,TGG | R132W | NP_001991.1 |
| NM_133269.3 | 555 | Missense Mutation | CGG,TGG | R132W | NP_579803.1 |
| NM_133271.3 | 555 | Intron | NP_579805.1 | ||
| NM_133272.3 | 555 | Missense Mutation | CGG,TGG | R120W | NP_579806.1 |
| NM_133273.3 | 555 | Intron | NP_579807.1 | ||
| NM_133274.3 | 555 | Missense Mutation | CGG,TGG | R120W | NP_579808.1 |
| NM_133277.3 | 555 | Missense Mutation | CGG,TGG | R23W | NP_579811.1 |
| NM_133278.3 | 555 | Missense Mutation | CGG,TGG | R120W | NP_579812.1 |
| XM_011526625.2 | 555 | Missense Mutation | CGG,TGG | R105W | XP_011524927.1 |
| XM_017026473.1 | 555 | Missense Mutation | CGG,TGG | R105W | XP_016881962.1 |
| XM_017026474.1 | 555 | Missense Mutation | CGG,TGG | R105W | XP_016881963.1 |