| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001100878.1 | 2153 | Missense Mutation | CGG,TGG | R608W | NP_001094348.1 |
| XM_006716615.2 | 2153 | Intron | XP_006716678.1 | ||
| XM_011517214.1 | 2153 | Missense Mutation | GCG,GTG | A693V | XP_011515516.1 |
| XM_011517215.1 | 2153 | Missense Mutation | GCG,GTG | A692V | XP_011515517.1 |
| XM_011517216.2 | 2153 | Missense Mutation | GCG,GTG | A693V | XP_011515518.1 |
| XM_011517217.1 | 2153 | Missense Mutation | GCG,GTG | A693V | XP_011515519.1 |
| XM_011517218.1 | 2153 | Missense Mutation | CGG,TGG | R569W | XP_011515520.1 |
| XM_011517219.1 | 2153 | UTR 3 | XP_011515521.1 | ||
| XM_011517220.1 | 2153 | UTR 3 | XP_011515522.1 | ||
| XM_011517221.2 | 2153 | Missense Mutation | CGG,TGG | R615W | XP_011515523.1 |
| XM_011517222.1 | 2153 | Missense Mutation | CGG,TGG | R615W | XP_011515524.1 |
| XM_011517223.1 | 2153 | Missense Mutation | CGG,TGG | R615W | XP_011515525.1 |