Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145306.2 | 772 | Missense Mutation | ACT,GCT | T21A | NP_660349.1 |
XM_005269606.1 | 772 | Missense Mutation | ACT,GCT | T63A | XP_005269663.1 |
XM_005269608.3 | 772 | Missense Mutation | ACT,GCT | T21A | XP_005269665.1 |
XM_011539455.2 | 772 | Missense Mutation | ACT,GCT | T21A | XP_011537757.1 |
XM_017015836.1 | 772 | Missense Mutation | ACT,GCT | T21A | XP_016871325.1 |