Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000670.4 | 1336 | Missense Mutation | ATC,GTC | I374V | NP_000661.2 |
NM_001306171.1 | 1336 | Missense Mutation | ATC,GTC | I393V | NP_001293100.1 |
NM_001306172.1 | 1336 | Missense Mutation | ATC,GTC | I393V | NP_001293101.1 |
XM_017007713.1 | 1336 | Intron | XP_016863202.1 | ||
XM_017007714.1 | 1336 | Intron | XP_016863203.1 | ||
XM_017007715.1 | 1336 | Intron | XP_016863204.1 |