| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193314.1 | 1449 | Missense Mutation | CTC,TTC | L484F | NP_001180243.1 |
| NM_001193315.1 | 1449 | Missense Mutation | CTC,TTC | L484F | NP_001180244.1 |
| NM_001193316.1 | 1449 | Missense Mutation | CTC,TTC | L435F | NP_001180245.1 |
| NM_001193317.1 | 1449 | Missense Mutation | CTC,TTC | L484F | NP_001180246.1 |
| NM_022067.3 | 1449 | Missense Mutation | CTC,TTC | L484F | NP_071350.2 |
| XM_011537066.1 | 1449 | Missense Mutation | CTC,TTC | L453F | XP_011535368.1 |
| XM_017021579.1 | 1449 | Missense Mutation | CTC,TTC | L453F | XP_016877068.1 |
| XM_017021580.1 | 1449 | Intron | XP_016877069.1 | ||
| XM_017021581.1 | 1449 | Intron | XP_016877070.1 |