Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080826.2 | 4495 | Missense Mutation | CGC,GGC | R1274G | NP_001074295.2 |
XM_005272369.4 | 4495 | Missense Mutation | CGC,GGC | R1274G | XP_005272426.2 |
XM_005272370.4 | 4495 | Missense Mutation | CGC,GGC | R1274G | XP_005272427.2 |
XM_011543813.2 | 4495 | Intron | XP_011542115.1 |