ENST00000261201.10:c.3783T>A
|
ENSP00000261201.4:p.Tyr1261Ter
|
|
ENST00000682426.1:n.1360T>A
|
|
|
ENST00000682879.1:c.*2881T>A
|
ENSP00000508210.1:n.*2881T>A
|
|
ENST00000683105.1:c.3771+854T>A
|
ENSP00000506801.1:n.3771+854T>A
|
|
ENST00000683676.1:c.3783T>A
|
ENSP00000508167.1:p.Tyr1261Ter
|
|
ENST00000683695.1:n.248T>A
|
|
|
ENST00000683811.1:n.4126T>A
|
|
|
ENST00000684084.1:c.3732T>A
|
ENSP00000507859.1:p.Tyr1244Ter
|
|
ENST00000261200.9:c.3783T>A
MANE Select
|
ENSP00000261200.4:p.Tyr1261Ter
|
|
ENST00000261201.9:c.3783T>A
|
ENSP00000261201.4:p.Tyr1261Ter
|
|
ENST00000261200.8:c.3783T>A
|
ENSP00000261200.4:p.Tyr1261Ter
|
|
ENST00000261201.8:c.3783T>A
|
ENSP00000261201.4:p.Tyr1261Ter
|
|
ENST00000544039.5:c.2664T>A
|
ENSP00000440521.1:p.Tyr888Ter
|
|
NM_005691.3:c.3783T>A
|
NP_005682.2:p.Tyr1261Ter
|
|
NM_020297.3:c.3783T>A
|
NP_064693.2:p.Tyr1261Ter
|
|
XM_005253284.2:c.3783T>A
|
XP_005253341.1:p.Tyr1261Ter
|
|
XM_005253286.2:c.3783T>A
|
XP_005253343.1:p.Tyr1261Ter
|
|
XM_005253287.3:c.3783T>A
|
XP_005253344.1:p.Tyr1261Ter
|
|
XM_005253288.2:c.3783T>A
|
XP_005253345.1:p.Tyr1261Ter
|
|
XM_005253289.2:c.3744T>A
|
XP_005253346.1:p.Tyr1248Ter
|
|
XM_005253290.2:c.3642T>A
|
XP_005253347.1:p.Tyr1214Ter
|
|
XM_006719025.2:c.3744T>A
|
XP_006719088.1:p.Tyr1248Ter
|
|
XM_011520545.1:c.3783T>A
|
XP_011518847.1:p.Tyr1261Ter
|
|
XR_931420.1:n.632-9914A>T
|
|
|
XR_931421.1:n.632-9914A>T
|
|
|
XR_931422.1:n.306-9914A>T
|
|
|
XM_005253284.4:c.3783T>A
|
XP_005253341.1:p.Tyr1261Ter
|
|
XM_005253286.4:c.3783T>A
|
XP_005253343.1:p.Tyr1261Ter
|
|
XM_005253287.5:c.3783T>A
|
XP_005253344.1:p.Tyr1261Ter
|
|
XM_005253288.4:c.3783T>A
|
XP_005253345.1:p.Tyr1261Ter
|
|
XM_005253289.4:c.3744T>A
|
XP_005253346.1:p.Tyr1248Ter
|
|
XM_005253290.4:c.3642T>A
|
XP_005253347.1:p.Tyr1214Ter
|
|
XM_006719025.4:c.3744T>A
|
XP_006719088.1:p.Tyr1248Ter
|
|
XM_011520545.3:c.3783T>A
|
XP_011518847.1:p.Tyr1261Ter
|
|
XR_931420.3:n.632-9914A>T
|
|
|
XR_931422.2:n.318-9914A>T
|
|
|
NM_001377273.1:c.3783T>A
|
NP_001364202.1:p.Tyr1261Ter
|
|
NM_001377274.1:c.2916T>A
|
NP_001364203.1:p.Tyr972Ter
|
|
NM_005691.4:c.3783T>A
|
NP_005682.2:p.Tyr1261Ter
|
|
NM_020297.4:c.3783T>A
MANE Select
|
NP_064693.2:p.Tyr1261Ter
|
|