| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001139443.1 | 751 | Intron | NP_001132915.1 | ||
| NM_001300786.1 | 751 | Intron | NP_001287715.1 | ||
| NM_001300787.1 | 751 | Intron | NP_001287716.1 | ||
| NM_004183.3 | 751 | Missense Mutation | CTG,GTG | L21V | NP_004174.1 |
| XM_005274210.3 | 751 | Missense Mutation | CTG,GTG | L21V | XP_005274267.1 |
| XM_005274215.3 | 751 | Intron | XP_005274272.1 | ||
| XM_005274216.3 | 751 | Intron | XP_005274273.1 | ||
| XM_005274219.3 | 751 | Missense Mutation | CTG,GTG | L21V | XP_005274276.1 |
| XM_005274221.3 | 751 | Missense Mutation | CTG,GTG | L21V | XP_005274278.1 |
| XM_011545229.2 | 751 | Missense Mutation | CTG,GTG | L21V | XP_011543531.1 |
| XM_011545230.2 | 751 | Intron | XP_011543532.1 | ||
| XM_011545233.2 | 751 | Intron | XP_011543535.1 | ||
| XM_017018228.1 | 751 | Intron | XP_016873717.1 | ||
| XM_017018229.1 | 751 | Missense Mutation | CTG,GTG | L21V | XP_016873718.1 |
| XM_017018230.1 | 751 | Intron | XP_016873719.1 |