Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000777.4 | 1710 | Missense Mutation | ACT,ATT | T488I | NP_000768.1 |
NM_001190484.2 | 1710 | Intron | NP_001177413.1 | ||
NM_001291829.1 | 1710 | Missense Mutation | ACT,ATT | T375I | NP_001278758.1 |
NM_001291830.1 | 1710 | Missense Mutation | ACT,ATT | T478I | NP_001278759.1 |
XM_006715859.2 | 1710 | Intron | XP_006715922.1 | ||
XM_011515843.1 | 1710 | Missense Mutation | ACT,ATT | T375I | XP_011514145.1 |
XM_017011781.1 | 1710 | Missense Mutation | ACT,ATT | T375I | XP_016867270.1 |
XM_017011782.1 | 1710 | Missense Mutation | ACT,ATT | T308I | XP_016867271.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145115.2 | 1710 | Intron | NP_660090.2 | ||
XM_005250194.2 | 1710 | Intron | XP_005250251.1 | ||
XM_011515905.2 | 1710 | Intron | XP_011514207.1 | ||
XM_011515906.2 | 1710 | Intron | XP_011514208.1 | ||
XM_011515907.2 | 1710 | Intron | XP_011514209.1 | ||
XM_011515908.2 | 1710 | Intron | XP_011514210.1 | ||
XM_011515909.2 | 1710 | Intron | XP_011514211.1 | ||
XM_011515910.2 | 1710 | Intron | XP_011514212.1 | ||
XM_017011824.1 | 1710 | Intron | XP_016867313.1 | ||
XM_017011825.1 | 1710 | Intron | XP_016867314.1 | ||
XM_017011826.1 | 1710 | Intron | XP_016867315.1 | ||
XM_017011827.1 | 1710 | Intron | XP_016867316.1 |