Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014614.2 | 5490 | Missense Mutation | ATG,GTG | M1800V | NP_055429.2 |
XM_006711969.1 | 5490 | Missense Mutation | ATG,GTG | M958V | XP_006712032.1 |
XM_011532705.2 | 5490 | Missense Mutation | ATG,GTG | M1826V | XP_011531007.1 |
XM_011532706.2 | 5490 | Missense Mutation | ATG,GTG | M1822V | XP_011531008.1 |
XM_011532707.2 | 5490 | Missense Mutation | ATG,GTG | M1804V | XP_011531009.1 |
XM_011532709.2 | 5490 | Intron | XP_011531011.1 |