Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024927.4 | 1849 | Missense Mutation | CTT,TTT | L516F | NP_079203.3 |
XM_017025113.1 | 1849 | Missense Mutation | CTT,TTT | L605F | XP_016880602.1 |
XM_017025114.1 | 1849 | Missense Mutation | CTT,TTT | L602F | XP_016880603.1 |
XM_017025115.1 | 1849 | Missense Mutation | CTT,TTT | L561F | XP_016880604.1 |
XM_017025116.1 | 1849 | Missense Mutation | CTT,TTT | L560F | XP_016880605.1 |
XM_017025117.1 | 1849 | Missense Mutation | CTT,TTT | L545F | XP_016880606.1 |
XM_017025118.1 | 1849 | Missense Mutation | CTT,TTT | L513F | XP_016880607.1 |