Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001306190.1 | 961 | Missense Mutation | ACG,ATG | T257M | NP_001293119.1 |
NM_001698.2 | 961 | Missense Mutation | ACG,ATG | T286M | NP_001689.1 |
XM_005252066.3 | 961 | Missense Mutation | ACG,ATG | T296M | XP_005252123.1 |
XM_005252067.4 | 961 | Missense Mutation | ACG,ATG | T296M | XP_005252124.1 |
XM_005252069.4 | 961 | Intron | XP_005252126.1 | ||
XM_005252072.2 | 961 | Intron | XP_005252129.1 | ||
XM_006717150.3 | 961 | Missense Mutation | ACG,ATG | T267M | XP_006717213.1 |
XM_011518800.2 | 961 | Intron | XP_011517102.1 | ||
XM_011518802.2 | 961 | Missense Mutation | ACG,ATG | T177M | XP_011517104.1 |
XM_011518803.2 | 961 | Intron | XP_011517105.1 | ||
XM_011518804.2 | 961 | Intron | XP_011517106.1 | ||
XM_017014849.1 | 961 | Missense Mutation | ACG,ATG | T286M | XP_016870338.1 |
XM_017014850.1 | 961 | Missense Mutation | ACG,ATG | T177M | XP_016870339.1 |
XM_017014851.1 | 961 | Missense Mutation | ACG,ATG | T177M | XP_016870340.1 |