Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_194296.1 | 488 | Missense Mutation | GCT,GTT | A154V | NP_919272.1 |
XM_005271916.4 | 488 | Missense Mutation | GCT,GTT | A154V | XP_005271973.1 |
XM_011543252.2 | 488 | Missense Mutation | GCT,GTT | A115V | XP_011541554.1 |
XM_011543253.2 | 488 | Missense Mutation | GCT,GTT | A115V | XP_011541555.1 |
XM_011543254.2 | 488 | Intron | XP_011541556.1 |