| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001258027.1 | 1779 | Intron | NP_001244956.1 | ||
| NM_001321308.1 | 1779 | Intron | NP_001308237.1 | ||
| NM_173535.2 | 1779 | Missense Mutation | CTG,GTG | L568V | NP_775806.2 |
| XM_011532635.2 | 1779 | Missense Mutation | CTG,GTG | L678V | XP_011530937.1 |
| XM_011532637.2 | 1779 | Missense Mutation | CTG,GTG | L678V | XP_011530939.1 |
| XM_011532638.2 | 1779 | Intron | XP_011530940.1 | ||
| XM_011532639.2 | 1779 | Intron | XP_011530941.1 | ||
| XM_011532640.2 | 1779 | Intron | XP_011530942.1 | ||
| XM_011532641.2 | 1779 | Intron | XP_011530943.1 | ||
| XM_011532642.2 | 1779 | Missense Mutation | CTG,GTG | L538V | XP_011530944.1 |
| XM_011532643.1 | 1779 | Missense Mutation | CTG,GTG | L507V | XP_011530945.1 |
| XM_017003519.1 | 1779 | Missense Mutation | CTG,GTG | L678V | XP_016859008.1 |