ENST00000556036.6:c.1566G>T
|
ENSP00000450596.1:p.Gln522His
|
|
ENST00000556250.6:c.1566G>T
|
ENSP00000452033.2:p.Gln522His
|
|
ENST00000696641.1:c.1407G>T
|
ENSP00000512774.1:p.Gln469His
|
|
ENST00000696642.1:c.*377G>T
|
ENSP00000512775.1:n.*377G>T
|
|
ENST00000696643.1:c.1566G>T
|
ENSP00000512776.1:p.Gln522His
|
|
ENST00000696646.1:c.*377G>T
|
ENSP00000512777.1:n.*377G>T
|
|
ENST00000696647.1:c.1566G>T
|
ENSP00000512778.1:p.Gln522His
|
|
ENST00000696648.1:c.1566G>T
|
ENSP00000512779.1:p.Gln522His
|
|
ENST00000696649.1:c.1566G>T
|
ENSP00000512780.1:p.Gln522His
|
|
ENST00000696650.1:n.1514G>T
|
|
|
ENST00000696658.1:n.2116G>T
|
|
|
ENST00000696662.1:c.1488G>T
|
ENSP00000512788.1:p.Gln496His
|
|
ENST00000696663.1:c.383G>T
|
|
|
ENST00000696664.1:c.383G>T
|
|
|
ENST00000696675.1:c.1566G>T
|
ENSP00000512799.1:p.Gln522His
|
|
ENST00000696680.1:c.1434G>T
|
ENSP00000512803.1:p.Gln478His
|
|
ENST00000696681.1:c.*377G>T
|
ENSP00000512804.1:n.*377G>T
|
|
ENST00000696682.1:c.1566G>T
|
ENSP00000512805.1:p.Gln522His
|
|
ENST00000696683.1:c.383G>T
|
|
|
ENST00000696684.1:c.383G>T
|
|
|
ENST00000696685.1:c.383G>T
|
|
|
ENST00000267430.10:c.1566G>T
MANE Select
|
ENSP00000267430.5:p.Gln522His
|
|
ENST00000267430.9:c.1566G>T
|
ENSP00000267430.5:p.Gln522His
|
|
ENST00000542564.6:c.1488G>T
|
ENSP00000442493.2:p.Gln496His
|
|
ENST00000556036.5:c.1566G>T
|
ENSP00000450596.1:p.Gln522His
|
|
ENST00000556250.5:c.321G>T
|
ENSP00000452033.1:p.Gln107His
|
|
NM_001308133.1:c.1488G>T
|
NP_001295062.1:p.Gln496His
|
|
NM_001308134.1:c.1566G>T
|
NP_001295063.1:p.Gln522His
|
|
NM_020937.2:c.1566G>T , LRG_502t1:c.1566G>T
|
NP_065988.1:p.Gln522His
|
|
NM_020937.3:c.1566G>T
|
NP_065988.1:p.Gln522His
|
|
XM_011537034.1:c.1566G>T
|
XP_011535336.1:p.Gln522His
|
|
XM_011537035.1:c.1488G>T
|
XP_011535337.1:p.Gln496His
|
|
XM_011537036.1:c.1566G>T
|
XP_011535338.1:p.Gln522His
|
|
XM_011537034.2:c.1566G>T
|
XP_011535336.1:p.Gln522His
|
|
XM_011537035.3:c.1488G>T
|
XP_011535337.1:p.Gln496His
|
|
XM_017021523.1:c.1566G>T
|
XP_016877012.1:p.Gln522His
|
|
XM_017021524.2:c.603G>T
|
XP_016877013.1:p.Gln201His
|
|
XM_017021525.2:c.381G>T
|
XP_016877014.1:p.Gln127His
|
|
XM_017021526.2:c.381G>T
|
XP_016877015.1:p.Gln127His
|
|
XM_017021527.1:c.381G>T
|
XP_016877016.1:p.Gln127His
|
|
XR_001750470.1:n.1658G>T
|
|
|
XR_001750471.2:n.1658G>T
|
|
|
XR_001750472.1:n.1658G>T
|
|
|
NM_020937.4:c.1566G>T
MANE Select
|
NP_065988.1:p.Gln522His
|
|
NM_001308133.2:c.1488G>T
|
NP_001295062.1:p.Gln496His
|
|
NM_001308134.2:c.1566G>T
|
NP_001295063.1:p.Gln522His
|
|