Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152550.3 | 522 | Missense Mutation | TTG,TTT | L96F | NP_689763.3 |
XM_005268380.2 | 522 | Missense Mutation | TTG,TTT | L96F | XP_005268437.1 |
XM_006714757.1 | 522 | Missense Mutation | TTG,TTT | L96F | XP_006714820.1 |
XM_011537567.2 | 522 | Missense Mutation | TTG,TTT | L96F | XP_011535869.1 |
XM_011537568.2 | 522 | Missense Mutation | TTG,TTT | L96F | XP_011535870.1 |
XM_011537569.2 | 522 | Missense Mutation | TTG,TTT | L96F | XP_011535871.1 |
XM_017009136.1 | 522 | Missense Mutation | TTG,TTT | L96F | XP_016864625.1 |