ENST00000224721.12:c.6413A>T
MANE Select
|
ENSP00000224721.9:p.Glu2138Val
|
|
ENST00000224721.10:c.6428A>T
|
ENSP00000224721.8:p.Glu2143Val
|
|
ENST00000622827.4:c.6413A>T
|
ENSP00000483211.1:p.Glu2138Val
|
|
NM_022124.5:c.6413A>T
|
NP_071407.4:p.Glu2138Val
|
|
XM_006717940.2:c.6608A>T
|
XP_006718003.1:p.Glu2203Val
|
|
XM_006717942.2:c.6542A>T
|
XP_006718005.1:p.Glu2181Val
|
|
XM_011540039.1:c.6605A>T
|
XP_011538341.1:p.Glu2202Val
|
|
XM_011540040.1:c.6602A>T
|
XP_011538342.1:p.Glu2201Val
|
|
XM_011540041.1:c.6548A>T
|
XP_011538343.1:p.Glu2183Val
|
|
XM_011540042.1:c.6577+31A>T
|
XP_011538344.1:n.6577+31A>T
|
|
XM_011540043.1:c.6608A>T
|
XP_011538345.1:p.Glu2203Val
|
|
XM_011540044.1:c.6473A>T
|
XP_011538346.1:p.Glu2158Val
|
|
XM_011540045.1:c.6608A>T
|
XP_011538347.1:p.Glu2203Val
|
|
XM_011540046.1:c.6068A>T
|
XP_011538348.1:p.Glu2023Val
|
|
XM_011540047.1:c.5426A>T
|
XP_011538349.1:p.Glu1809Val
|
|
XM_011540048.1:c.6608A>T
|
XP_011538350.1:p.Glu2203Val
|
|
XM_011540049.1:c.6608A>T
|
XP_011538351.1:p.Glu2203Val
|
|
XM_011540050.1:c.6608A>T
|
XP_011538352.1:p.Glu2203Val
|
|
XM_011540051.1:c.6608A>T
|
XP_011538353.1:p.Glu2203Val
|
|
XM_011540052.1:c.2936A>T
|
XP_011538354.1:p.Glu979Val
|
|
XR_945796.1:n.6851A>T
|
|
|
NM_022124.6:c.6413A>T
MANE Select
|
NP_071407.4:p.Glu2138Val
|
|