Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142603.2 | 332 | Missense Mutation | AGG,GGG | R59G | NP_001136075.1 |
NM_014773.4 | 332 | Missense Mutation | AGG,GGG | R59G | NP_055588.3 |
XM_005268547.3 | 332 | Missense Mutation | AGG,GGG | R59G | XP_005268604.1 |
XM_005268548.3 | 332 | Missense Mutation | AGG,GGG | R59G | XP_005268605.1 |
XM_005268552.2 | 332 | Missense Mutation | AGG,GGG | R59G | XP_005268609.1 |
XM_006714812.3 | 332 | Intron | XP_006714875.1 | ||
XM_011537715.1 | 332 | Missense Mutation | AGG,GGG | R59G | XP_011536017.1 |
XM_011537716.2 | 332 | Missense Mutation | AGG,GGG | R59G | XP_011536018.1 |