Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098526.1 | 1269 | Missense Mutation | GCA,GGA | A386G | NP_001091996.1 |
NM_001286570.1 | 1269 | Missense Mutation | GCA,GGA | A347G | NP_001273499.1 |
NM_001286571.1 | 1269 | Missense Mutation | GCA,GGA | A347G | NP_001273500.1 |
NM_153206.2 | 1269 | Missense Mutation | GCA,GGA | A376G | NP_694938.2 |
XM_005271407.3 | 1269 | Missense Mutation | GCA,GGA | A376G | XP_005271464.1 |
XM_017017213.1 | 1269 | Missense Mutation | GCA,GGA | A408G | XP_016872702.1 |
XM_017017214.1 | 1269 | Missense Mutation | GCA,GGA | A253G | XP_016872703.1 |
XM_017017215.1 | 1269 | Missense Mutation | GCA,GGA | A253G | XP_016872704.1 |