| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142351.1 | 1650 | Missense Mutation | CTT,GTT | L511V | NP_001135823.1 |
| NM_001142352.1 | 1650 | Intron | NP_001135824.1 | ||
| NM_001322362.1 | 1650 | Missense Mutation | CTT,GTT | L511V | NP_001309291.1 |
| NM_032528.2 | 1650 | Missense Mutation | CTT,GTT | L511V | NP_115917.1 |
| XM_006712802.1 | 1650 | Missense Mutation | CTT,GTT | L511V | XP_006712865.1 |
| XM_011511999.2 | 1650 | Missense Mutation | CTT,GTT | L511V | XP_011510301.1 |
| XM_011512000.2 | 1650 | Intron | XP_011510302.1 | ||
| XM_011512001.2 | 1650 | Intron | XP_011510303.1 | ||
| XM_017005110.1 | 1650 | Intron | XP_016860599.1 |