Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000233.3 | 1798 | Missense Mutation | ACT,CCT | T668P | NP_000224.2 |
XM_005264309.3 | 1798 | Missense Mutation | ACT,CCT | T349P | XP_005264366.1 |
XM_006712015.3 | 1798 | Missense Mutation | ACT,CCT | T358P | XP_006712078.1 |
XM_011532828.1 | 1798 | Missense Mutation | ACT,CCT | T643P | XP_011531130.1 |
XM_011532831.1 | 1798 | Missense Mutation | ACT,CCT | T456P | XP_011531133.1 |
XM_011532834.2 | 1798 | Missense Mutation | ACT,CCT | T349P | XP_011531136.1 |
XM_017004089.1 | 1798 | Missense Mutation | ACT,CCT | T583P | XP_016859578.1 |
XM_017004090.1 | 1798 | Missense Mutation | ACT,CCT | T456P | XP_016859579.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198593.1 | 1798 | Intron | NP_001185522.1 | ||
NM_001198594.1 | 1798 | Intron | NP_001185523.1 | ||
NM_172311.2 | 1798 | Intron | NP_758515.1 |