Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_153046.2 | 171 | Silent Mutation | CTG,TTG | L2L | NP_694591.2 |
XM_005267309.3 | 171 | Missense Mutation | CTG,TTG | L2L | XP_005267366.1 |
XM_006720019.3 | 171 | Missense Mutation | CTG,TTG | L2L | XP_006720082.1 |
XM_006720020.3 | 171 | Missense Mutation | CTG,TTG | L2L | XP_006720083.1 |
XM_011536397.2 | 171 | Missense Mutation | CTG,TTG | L2L | XP_011534699.1 |
XM_011536398.2 | 171 | Intron | XP_011534700.1 | ||
XM_011536400.2 | 171 | Silent Mutation | CTG,TTG | L2L | XP_011534702.1 |
XM_011536401.2 | 171 | Intron | XP_011534703.1 | ||
XM_011536402.2 | 171 | Intron | XP_011534704.1 | ||
XM_017020955.1 | 171 | UTR 5 | XP_016876444.1 |