| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_138697.3 | 190 | Intron | NP_619642.2 | ||
| NM_177540.2 | 190 | Intron | NP_803884.1 | ||
| XM_011542203.2 | 190 | Intron | XP_011540505.1 | ||
| XM_011542206.2 | 190 | Intron | XP_011540508.1 | ||
| XM_017002402.1 | 190 | Intron | XP_016857891.1 | ||
| XM_017002403.1 | 190 | Intron | XP_016857892.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278647.1 | 190 | Missense Mutation | CAG,CTG | Q14L | NP_001265576.1 |
| NM_001278648.1 | 190 | Missense Mutation | CAG,CTG | Q14L | NP_001265577.1 |
| NM_005341.3 | 190 | Missense Mutation | CAG,CTG | Q14L | NP_005332.1 |
| XM_017001110.1 | 190 | Missense Mutation | CAG,CTG | Q14L | XP_016856599.1 |
| XM_017001111.1 | 190 | Missense Mutation | CAG,CTG | Q14L | XP_016856600.1 |
| XM_017001112.1 | 190 | UTR 5 | XP_016856601.1 | ||
| XM_017001113.1 | 190 | UTR 5 | XP_016856602.1 | ||
| XM_017001114.1 | 190 | UTR 5 | XP_016856603.1 |