ENST00000312428.11:c.10748G>A
MANE Select
|
ENSP00000311273.6:p.Cys3583Tyr
|
|
ENST00000312428.10:c.10748G>A
|
ENSP00000311273.6:p.Cys3583Tyr
|
|
ENST00000409063.5:c.197G>A
|
ENSP00000386912.1:p.Cys66Tyr
|
|
NM_018897.2:c.10748G>A
|
NP_061720.2:p.Cys3583Tyr
|
|
XM_011511487.1:c.10748G>A
|
XP_011509789.1:p.Cys3583Tyr
|
|
XM_011511488.1:c.10628G>A
|
XP_011509790.1:p.Cys3543Tyr
|
|
XM_011511489.1:c.10610G>A
|
XP_011509791.1:p.Cys3537Tyr
|
|
XM_011511490.1:c.10523G>A
|
XP_011509792.1:p.Cys3508Tyr
|
|
XM_011511496.1:c.6392G>A
|
XP_011509798.1:p.Cys2131Tyr
|
|
XM_011511497.1:c.5120G>A
|
XP_011509799.1:p.Cys1707Tyr
|
|
XM_011511488.3:c.10628G>A
|
XP_011509790.1:p.Cys3543Tyr
|
|
XM_011511489.2:c.10610G>A
|
XP_011509791.1:p.Cys3537Tyr
|
|
XM_011511490.3:c.10523G>A
|
XP_011509792.1:p.Cys3508Tyr
|
|
XM_011511497.2:c.5120G>A
|
XP_011509799.1:p.Cys1707Tyr
|
|
XM_017004504.2:c.10475G>A
|
XP_016859993.1:p.Cys3492Tyr
|
|
NM_018897.3:c.10748G>A
MANE Select
|
NP_061720.2:p.Cys3583Tyr
|
|