Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_144622.2 | 1620 | Missense Mutation | CTC,TTC | L693F | NP_653223.2 |
XM_011509188.2 | 1620 | Missense Mutation | CTC,TTC | L473F | XP_011507490.1 |
XM_011509189.2 | 1620 | Missense Mutation | CTC,TTC | L361F | XP_011507491.1 |