| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143682.1 | 1811 | Missense Mutation | CTG,GTG | L443V | NP_001137154.1 |
| NM_020898.2 | 1811 | Missense Mutation | CTG,GTG | L528V | NP_065949.1 |
| XM_011538601.1 | 1811 | Missense Mutation | CTG,GTG | L528V | XP_011536903.1 |
| XM_011538602.1 | 1811 | Missense Mutation | CTG,GTG | L528V | XP_011536904.1 |
| XM_011538603.1 | 1811 | Missense Mutation | CTG,GTG | L528V | XP_011536905.1 |
| XM_011538604.1 | 1811 | Missense Mutation | CTG,GTG | L528V | XP_011536906.1 |
| XM_017019707.1 | 1811 | Missense Mutation | CTG,GTG | L528V | XP_016875196.1 |
| XM_017019708.1 | 1811 | Missense Mutation | CTG,GTG | L205V | XP_016875197.1 |
| XM_017019709.1 | 1811 | Missense Mutation | CTG,GTG | L205V | XP_016875198.1 |