| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_199289.2 | 2089 | Missense Mutation | CTT,TTT | L643F | NP_954983.1 |
| XM_006719808.3 | 2089 | Intron | XP_006719871.2 | ||
| XM_011535066.2 | 2089 | Intron | XP_011533368.1 | ||
| XM_011535068.2 | 2089 | Intron | XP_011533370.1 | ||
| XM_017020555.1 | 2089 | Missense Mutation | CTT,TTT | L690F | XP_016876044.1 |
| XM_017020556.1 | 2089 | Intron | XP_016876045.1 | ||
| XM_017020557.1 | 2089 | Missense Mutation | CTT,TTT | L715F | XP_016876046.1 |