Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136043.2 | 1730 | Missense Mutation | GCC,GGC | A413G | NP_001129515.1 |
NM_001207058.1 | 1730 | Missense Mutation | GCC,GGC | A474G | NP_001193987.1 |
NM_001207059.1 | 1730 | Missense Mutation | GCC,GGC | A435G | NP_001193988.1 |
XM_006720708.3 | 1730 | Missense Mutation | GCC,GGC | A524G | XP_006720771.1 |
XM_006720709.3 | 1730 | Missense Mutation | GCC,GGC | A413G | XP_006720772.1 |
XM_006720711.2 | 1730 | Missense Mutation | GCC,GGC | A413G | XP_006720774.1 |
XM_011522101.2 | 1730 | Missense Mutation | GCC,GGC | A413G | XP_011520403.1 |
XM_017022644.1 | 1730 | Missense Mutation | GCC,GGC | A413G | XP_016878133.1 |