Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001447.2 | 13231 | Missense Mutation | AGG,GGG | R4293G | NP_001438.1 |
XM_006714761.3 | 13231 | Missense Mutation | AGG,GGG | R4293G | XP_006714824.1 |
XM_011537600.2 | 13231 | Missense Mutation | AGG,GGG | R4293G | XP_011535902.1 |
XM_011537603.2 | 13231 | Missense Mutation | AGG,GGG | R4293G | XP_011535905.1 |
XM_017009224.1 | 13231 | Missense Mutation | AGG,GGG | R4293G | XP_016864713.1 |
XM_017009225.1 | 13231 | Missense Mutation | AGG,GGG | R4293G | XP_016864714.1 |
XM_017009226.1 | 13231 | Intron | XP_016864715.1 | ||
XM_017009227.1 | 13231 | Intron | XP_016864716.1 |