Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000390.3 | 1670 | Silent Mutation | CTG,CTT | L547L | NP_000381.1 |
NM_001145414.3 | 1670 | Intron | NP_001138886.1 | ||
NM_001320959.1 | 1670 | Silent Mutation | CTG,CTT | L399L | NP_001307888.1 |
XM_017029242.1 | 1670 | Silent Mutation | CTG,CTT | L547L | XP_016884731.1 |
XM_017029243.1 | 1670 | Silent Mutation | CTG,CTT | L399L | XP_016884732.1 |
XM_017029244.1 | 1670 | Silent Mutation | CTG,CTT | L399L | XP_016884733.1 |
XM_017029245.1 | 1670 | Silent Mutation | CTG,CTT | L399L | XP_016884734.1 |
XM_017029246.1 | 1670 | Silent Mutation | CTG,CTT | L399L | XP_016884735.1 |