Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152512.3 | 1627 | Silent Mutation | CTG,TTG | L449L | NP_689725.2 |
XM_006724149.3 | 1627 | Silent Mutation | CTG,TTG | L449L | XP_006724212.1 |
XM_006724150.3 | 1627 | Silent Mutation | CTG,TTG | L396L | XP_006724213.1 |
XM_006724151.1 | 1627 | Silent Mutation | CTG,TTG | L336L | XP_006724214.1 |
XM_006724153.3 | 1627 | Intron | XP_006724216.1 | ||
XM_011529927.2 | 1627 | Silent Mutation | CTG,TTG | L428L | XP_011528229.1 |
XM_011529928.2 | 1627 | Silent Mutation | CTG,TTG | L368L | XP_011528230.1 |
XM_011529930.2 | 1627 | Silent Mutation | CTG,TTG | L185L | XP_011528232.1 |
XM_011529931.2 | 1627 | Intron | XP_011528233.1 |