ENST00000333213.11:c.1505T>A
MANE Select
|
ENSP00000327487.6:p.Phe502Tyr
|
|
ENST00000434205.8:c.1202T>A
|
ENSP00000406559.4:p.Phe401Tyr
|
|
ENST00000545228.3:c.*4T>A
|
ENSP00000438169.3:n.*4T>A
|
|
ENST00000577197.2:n.703T>A
|
|
|
ENST00000579449.2:n.2245T>A
|
|
|
ENST00000580013.6:n.2649T>A
|
|
|
ENST00000679370.1:n.3027T>A
|
|
|
ENST00000679429.1:c.*963T>A
|
ENSP00000505403.1:n.*963T>A
|
|
ENST00000679443.1:n.1574T>A
|
|
|
ENST00000679782.1:c.*204T>A
|
ENSP00000505995.1:n.*204T>A
|
|
ENST00000679919.1:n.1776T>A
|
|
|
ENST00000679928.1:c.*2057T>A
|
ENSP00000506071.1:n.*2057T>A
|
|
ENST00000680528.1:n.2471T>A
|
|
|
ENST00000680999.1:c.1718T>A
|
ENSP00000504984.1:p.Phe573Tyr
|
|
ENST00000681282.1:c.*1692T>A
|
ENSP00000506339.1:n.*1692T>A
|
|
ENST00000333213.10:c.1505T>A
|
ENSP00000327487.6:p.Phe502Tyr
|
|
ENST00000545228.2:c.782T>A
|
|
|
ENST00000577197.1:n.253T>A
|
|
|
ENST00000579449.1:n.702T>A
|
|
|
NM_207346.2:c.1505T>A
|
NP_997229.2:p.Phe502Tyr
|
|
XM_005257229.2:c.*4T>A
|
XP_005257286.1:n.*4T>A
|
|
XM_006721821.2:c.*4T>A
|
XP_006721884.1:n.*4T>A
|
|
XM_011524616.1:c.*4T>A
|
XP_011522918.1:n.*4T>A
|
|
XM_011524617.1:c.*87T>A
|
XP_011522919.1:n.*87T>A
|
|
XM_011524618.1:c.1388T>A
|
XP_011522920.1:p.Phe463Tyr
|
|
XR_243646.2:n.1737T>A
|
|
|
XM_005257229.4:c.*4T>A
|
XP_005257286.1:n.*4T>A
|
|
XR_001753015.1:n.62A>T
|
|
|
XR_001753016.1:n.63A>T
|
|
|
XR_243646.4:n.1743T>A
|
|
|
NM_207346.3:c.1505T>A
MANE Select
|
NP_997229.2:p.Phe502Tyr
|
|