Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080826.2 | 3838 | Missense Mutation | ATC,GTC | I1055V | NP_001074295.2 |
XM_005272369.4 | 3838 | Missense Mutation | ATC,GTC | I1055V | XP_005272426.2 |
XM_005272370.4 | 3838 | Missense Mutation | ATC,GTC | I1055V | XP_005272427.2 |
XM_011543813.2 | 3838 | Intron | XP_011542115.1 |