Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302826.1 | 1012 | Silent Mutation | CTG,CTT | L263L | NP_001289755.1 |
NM_001302827.1 | 1012 | UTR 3 | NP_001289756.1 | ||
NM_016229.4 | 1012 | Silent Mutation | CTG,CTT | L263L | NP_057313.2 |
XM_005252975.4 | 1012 | Silent Mutation | CTG,CTT | L263L | XP_005253032.1 |
XM_006718251.2 | 1012 | Silent Mutation | CTG,CTT | L263L | XP_006718314.1 |
XM_011520184.2 | 1012 | Silent Mutation | CTG,CTT | L323L | XP_011518486.1 |
XM_011520185.2 | 1012 | UTR 3 | XP_011518487.1 | ||
XM_017017920.1 | 1012 | Silent Mutation | CTG,CTT | L323L | XP_016873409.1 |
XM_017017921.1 | 1012 | UTR 3 | XP_016873410.1 | ||
XM_017017922.1 | 1012 | UTR 3 | XP_016873411.1 |