ENST00000333213.11:c.1454T>A
MANE Select
|
ENSP00000327487.6:p.Leu485His
|
|
ENST00000434205.8:c.1151T>A
|
ENSP00000406559.4:p.Leu384His
|
|
ENST00000545228.3:c.1642T>A
|
ENSP00000438169.3:p.Ser548Thr
|
|
ENST00000577197.2:n.652T>A
|
|
|
ENST00000579449.2:n.2194T>A
|
|
|
ENST00000580013.6:n.2598T>A
|
|
|
ENST00000679370.1:n.2976T>A
|
|
|
ENST00000679429.1:c.*912T>A
|
ENSP00000505403.1:n.*912T>A
|
|
ENST00000679443.1:n.1523T>A
|
|
|
ENST00000679782.1:c.*153T>A
|
ENSP00000505995.1:n.*153T>A
|
|
ENST00000679919.1:n.1725T>A
|
|
|
ENST00000679928.1:c.*2006T>A
|
ENSP00000506071.1:n.*2006T>A
|
|
ENST00000680528.1:n.2420T>A
|
|
|
ENST00000680999.1:c.1667T>A
|
ENSP00000504984.1:p.Leu556His
|
|
ENST00000681282.1:c.*1641T>A
|
ENSP00000506339.1:n.*1641T>A
|
|
ENST00000333213.10:c.1454T>A
|
ENSP00000327487.6:p.Leu485His
|
|
ENST00000545228.2:c.731T>A
|
|
|
ENST00000577197.1:n.202T>A
|
|
|
ENST00000579449.1:n.651T>A
|
|
|
NM_207346.2:c.1454T>A
|
NP_997229.2:p.Leu485His
|
|
XM_005257229.2:c.1642T>A
|
XP_005257286.1:p.Ser548Thr
|
|
XM_006721821.2:c.1339T>A
|
XP_006721884.1:p.Ser447Thr
|
|
XM_011524616.1:c.1525T>A
|
XP_011522918.1:p.Ser509Thr
|
|
XM_011524617.1:c.*36T>A
|
XP_011522919.1:n.*36T>A
|
|
XM_011524618.1:c.1337T>A
|
XP_011522920.1:p.Leu446His
|
|
XR_243646.2:n.1686T>A
|
|
|
XM_005257229.4:c.1642T>A
|
XP_005257286.1:p.Ser548Thr
|
|
XR_001753015.1:n.87+26A>T
|
|
|
XR_001753016.1:n.88+26A>T
|
|
|
XR_243646.4:n.1692T>A
|
|
|
NM_207346.3:c.1454T>A
MANE Select
|
NP_997229.2:p.Leu485His
|
|