ENST00000333213.11:c.1434T>A
MANE Select
|
ENSP00000327487.6:p.Phe478Leu
|
|
ENST00000434205.8:c.1131T>A
|
ENSP00000406559.4:p.Phe377Leu
|
|
ENST00000545228.3:c.1622T>A
|
ENSP00000438169.3:p.Leu541Ter
|
|
ENST00000577197.2:n.632T>A
|
|
|
ENST00000579449.2:n.2174T>A
|
|
|
ENST00000580013.6:n.2578T>A
|
|
|
ENST00000679370.1:n.2956T>A
|
|
|
ENST00000679429.1:c.*892T>A
|
ENSP00000505403.1:n.*892T>A
|
|
ENST00000679443.1:n.1503T>A
|
|
|
ENST00000679782.1:c.*133T>A
|
ENSP00000505995.1:n.*133T>A
|
|
ENST00000679919.1:n.1705T>A
|
|
|
ENST00000679928.1:c.*1986T>A
|
ENSP00000506071.1:n.*1986T>A
|
|
ENST00000680528.1:n.2400T>A
|
|
|
ENST00000680999.1:c.1647T>A
|
ENSP00000504984.1:p.Phe549Leu
|
|
ENST00000681282.1:c.*1621T>A
|
ENSP00000506339.1:n.*1621T>A
|
|
ENST00000333213.10:c.1434T>A
|
ENSP00000327487.6:p.Phe478Leu
|
|
ENST00000545228.2:c.711T>A
|
|
|
ENST00000577197.1:n.182T>A
|
|
|
ENST00000579449.1:n.631T>A
|
|
|
NM_207346.2:c.1434T>A
|
NP_997229.2:p.Phe478Leu
|
|
XM_005257229.2:c.1622T>A
|
XP_005257286.1:p.Leu541Ter
|
|
XM_006721821.2:c.1319T>A
|
XP_006721884.1:p.Leu440Ter
|
|
XM_011524616.1:c.1505T>A
|
XP_011522918.1:p.Leu502Ter
|
|
XM_011524617.1:c.*16T>A
|
XP_011522919.1:n.*16T>A
|
|
XM_011524618.1:c.1317T>A
|
XP_011522920.1:p.Phe439Leu
|
|
XR_243646.2:n.1666T>A
|
|
|
XM_005257229.4:c.1622T>A
|
XP_005257286.1:p.Leu541Ter
|
|
XR_001753015.1:n.87+46A>T
|
|
|
XR_001753016.1:n.88+46A>T
|
|
|
XR_243646.4:n.1672T>A
|
|
|
NM_207346.3:c.1434T>A
MANE Select
|
NP_997229.2:p.Phe478Leu
|
|