Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152357.2 | 1622 | Missense Mutation | CTT,TTT | L530F | NP_689570.2 |
XM_005259731.3 | 1622 | Missense Mutation | CTT,TTT | L533F | XP_005259788.1 |
XM_017026253.1 | 1622 | Missense Mutation | CTT,TTT | L532F | XP_016881742.1 |
XM_017026254.1 | 1622 | Missense Mutation | CTT,TTT | L408F | XP_016881743.1 |