|
ENST00000646891.2:c.1784T>G
MANE Select
|
ENSP00000493543.1:p.Phe595Cys
|
|
|
ENST00000288602.11:c.1904T>G
|
ENSP00000288602.7:p.Phe635Cys
|
|
|
ENST00000479537.6:c.454T>G
|
|
|
|
ENST00000496384.7:c.1784T>G
|
ENSP00000419060.2:p.Phe595Cys
|
|
|
ENST00000497784.2:c.*1234T>G
|
ENSP00000420119.2:n.*1234T>G
|
|
|
ENST00000642228.1:c.*862T>G
|
ENSP00000493678.1:n.*862T>G
|
|
|
ENST00000642875.1:n.1259-3933T>G
|
|
|
|
ENST00000644120.1:n.2174T>G
|
|
|
|
ENST00000644650.1:c.880T>G
|
|
|
|
ENST00000644905.1:n.2666T>G
|
|
|
|
ENST00000644969.2:c.1904T>G
MANE Plus Clinical
|
ENSP00000496776.1:p.Phe635Cys
|
|
|
ENST00000646730.1:c.*360T>G
|
ENSP00000494784.1:n.*360T>G
|
|
|
ENST00000646891.1:c.1784T>G
|
ENSP00000493543.1:p.Phe595Cys
|
|
|
ENST00000647434.1:c.738-3933T>G
|
ENSP00000495132.1:n.738-3933T>G
|
|
|
ENST00000288602.10:c.1784T>G
|
ENSP00000288602.6:p.Phe595Cys
|
|
|
ENST00000479537.5:c.68T>G
|
ENSP00000418033.1:p.Phe23Cys
|
|
|
ENST00000496384.6:c.607T>G
|
|
|
|
ENST00000497784.1:c.1819T>G
|
ENSP00000420119.1:n.1819T>G
|
|
|
NM_004333.4:c.1784T>G , LRG_299t1:c.1784T>G
|
NP_004324.2:p.Phe595Cys
|
|
|
XM_005250045.1:c.1784T>G
|
XP_005250102.1:p.Phe595Cys
|
|
|
XM_005250046.1:c.1784T>G
|
XP_005250103.1:p.Phe595Cys
|
|
|
XM_011516529.1:c.1784T>G
|
XP_011514831.1:p.Phe595Cys
|
|
|
XM_011516530.1:c.1695-3933T>G
|
XP_011514832.1:n.1695-3933T>G
|
|
|
XR_242190.1:n.1792T>G
|
|
|
|
XR_927520.1:n.1792T>G
|
|
|
|
XR_927521.1:n.1792T>G
|
|
|
|
XR_927522.1:n.1703-3933T>G
|
|
|
|
XR_927523.1:n.1703-3933T>G
|
|
|
|
NM_001354609.1:c.1784T>G
|
NP_001341538.1:p.Phe595Cys
|
|
|
NM_004333.5:c.1784T>G
|
NP_004324.2:p.Phe595Cys
|
|
|
NR_148928.1:n.2882T>G
|
|
|
|
XM_017012558.1:c.1904T>G
|
XP_016868047.1:p.Phe635Cys
|
|
|
XM_017012559.1:c.1904T>G
|
XP_016868048.1:p.Phe635Cys
|
|
|
XR_001744857.1:n.1912T>G
|
|
|
|
XR_001744858.1:n.1823-3933T>G
|
|
|
|
NM_001354609.2:c.1784T>G
|
NP_001341538.1:p.Phe595Cys
|
|
|
NM_001374244.1:c.1904T>G
|
NP_001361173.1:p.Phe635Cys
|
|
|
NM_001374258.1:c.1904T>G
MANE Plus Clinical
|
NP_001361187.1:p.Phe635Cys
|
|
|
NM_004333.6:c.1784T>G
MANE Select
|
NP_004324.2:p.Phe595Cys
|
|
|
NM_001378467.1:c.1793T>G
|
NP_001365396.1:p.Phe598Cys
|
|
|
NM_001378468.1:c.1784T>G
|
NP_001365397.1:p.Phe595Cys
|
|
|
NM_001378469.1:c.1718T>G
|
NP_001365398.1:p.Phe573Cys
|
|
|
NM_001378470.1:c.1682T>G
|
NP_001365399.1:p.Phe561Cys
|
|
|
NM_001378471.1:c.1673T>G
|
NP_001365400.1:p.Phe558Cys
|
|
|
NM_001378472.1:c.1628T>G
|
NP_001365401.1:p.Phe543Cys
|
|
|
NM_001378473.1:c.1628T>G
|
NP_001365402.1:p.Phe543Cys
|
|
|
NM_001378474.1:c.1784T>G
|
NP_001365403.1:p.Phe595Cys
|
|
|
NM_001378475.1:c.1520T>G
|
NP_001365404.1:p.Phe507Cys
|
|
