Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005744.3 | 479 | Silent Mutation | GGC,GGT | G55G | NP_005735.2 |
XM_011521438.2 | 479 | Missense Mutation | GCG,GTG | A19V | XP_011519740.1 |
XM_011521439.2 | 479 | Intron | XP_011519741.1 |