ENST00000333213.11:c.1439A>T
MANE Select
|
ENSP00000327487.6:p.Glu480Val
|
|
ENST00000434205.8:c.1136A>T
|
ENSP00000406559.4:p.Glu379Val
|
|
ENST00000545228.3:c.1627A>T
|
ENSP00000438169.3:p.Ser543Cys
|
|
ENST00000577197.2:n.637A>T
|
|
|
ENST00000579449.2:n.2179A>T
|
|
|
ENST00000580013.6:n.2583A>T
|
|
|
ENST00000679370.1:n.2961A>T
|
|
|
ENST00000679429.1:c.*897A>T
|
ENSP00000505403.1:n.*897A>T
|
|
ENST00000679443.1:n.1508A>T
|
|
|
ENST00000679782.1:c.*138A>T
|
ENSP00000505995.1:n.*138A>T
|
|
ENST00000679919.1:n.1710A>T
|
|
|
ENST00000679928.1:c.*1991A>T
|
ENSP00000506071.1:n.*1991A>T
|
|
ENST00000680528.1:n.2405A>T
|
|
|
ENST00000680999.1:c.1652A>T
|
ENSP00000504984.1:p.Glu551Val
|
|
ENST00000681282.1:c.*1626A>T
|
ENSP00000506339.1:n.*1626A>T
|
|
ENST00000333213.10:c.1439A>T
|
ENSP00000327487.6:p.Glu480Val
|
|
ENST00000545228.2:c.716A>T
|
|
|
ENST00000577197.1:n.187A>T
|
|
|
ENST00000579449.1:n.636A>T
|
|
|
NM_207346.2:c.1439A>T
|
NP_997229.2:p.Glu480Val
|
|
XM_005257229.2:c.1627A>T
|
XP_005257286.1:p.Ser543Cys
|
|
XM_006721821.2:c.1324A>T
|
XP_006721884.1:p.Ser442Cys
|
|
XM_011524616.1:c.1510A>T
|
XP_011522918.1:p.Ser504Cys
|
|
XM_011524617.1:c.*21A>T
|
XP_011522919.1:n.*21A>T
|
|
XM_011524618.1:c.1322A>T
|
XP_011522920.1:p.Glu441Val
|
|
XR_243646.2:n.1671A>T
|
|
|
XM_005257229.4:c.1627A>T
|
XP_005257286.1:p.Ser543Cys
|
|
XR_001753015.1:n.87+41T>A
|
|
|
XR_001753016.1:n.88+41T>A
|
|
|
XR_243646.4:n.1677A>T
|
|
|
NM_207346.3:c.1439A>T
MANE Select
|
NP_997229.2:p.Glu480Val
|
|