Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_030809.2 | 1749 | Missense Mutation | CTC,GTC | L508V | NP_110436.1 |
XM_006719621.2 | 1749 | Missense Mutation | CTC,GTC | L508V | XP_006719684.1 |
XM_017019991.1 | 1749 | Missense Mutation | CTC,GTC | L269V | XP_016875480.1 |