Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001085354.2 | 2199 | Missense Mutation | GTT,TTT | V642F | NP_001078823.1 |
NM_024657.4 | 2199 | Missense Mutation | GTT,TTT | V642F | NP_078933.3 |
XM_005262190.3 | 2199 | Missense Mutation | GTT,TTT | V550F | XP_005262247.1 |
XM_006724691.2 | 2199 | Missense Mutation | GTT,TTT | V520F | XP_006724754.1 |
XM_011531027.2 | 2199 | Missense Mutation | GTT,TTT | V465F | XP_011529329.1 |
XM_017029844.1 | 2199 | Missense Mutation | GTT,TTT | V550F | XP_016885333.1 |