ENST00000264932.11:c.1529A>T
MANE Select
|
ENSP00000264932.6:p.Glu510Val
|
|
ENST00000651543.1:c.*262A>T
|
ENSP00000499215.1:n.*262A>T
|
|
ENST00000264932.10:c.1529A>T
|
ENSP00000264932.6:p.Glu510Val
|
|
ENST00000504309.5:c.1529A>T
|
ENSP00000426514.1:p.Glu510Val
|
|
ENST00000505555.5:n.1569A>T
|
|
|
ENST00000509082.1:n.11A>T
|
|
|
ENST00000510361.5:c.1385A>T
|
ENSP00000427703.1:p.Glu462Val
|
|
ENST00000511810.5:n.2276A>T
|
|
|
ENST00000514027.5:n.1484A>T
|
|
|
ENST00000515752.5:n.1115A>T
|
|
|
ENST00000515815.5:c.184A>T
|
|
|
ENST00000617470.4:c.1094A>T
|
ENSP00000484230.1:p.Glu365Val
|
|
NM_001294332.1:c.1385A>T
|
NP_001281261.1:p.Glu462Val
|
|
NM_004168.3:c.1529A>T
|
NP_004159.2:p.Glu510Val
|
|
XM_005248331.2:c.1529A>T
|
XP_005248388.1:p.Glu510Val
|
|
XM_011514072.1:c.1529A>T
|
XP_011512374.1:p.Glu510Val
|
|
XM_011514073.1:c.1529A>T
|
XP_011512375.1:p.Glu510Val
|
|
XR_925638.1:n.1662A>T
|
|
|
NM_001330758.1:c.1529A>T
|
NP_001317687.1:p.Glu510Val
|
|
XM_011514072.2:c.1529A>T
|
XP_011512374.1:p.Glu510Val
|
|
XM_011514073.2:c.1529A>T
|
XP_011512375.1:p.Glu510Val
|
|
XM_017009685.2:c.1529A>T
|
XP_016865174.1:p.Glu510Val
|
|
XM_024446143.1:c.1385A>T
|
XP_024301911.1:p.Glu462Val
|
|
XR_002956167.1:n.1576A>T
|
|
|
NM_004168.4:c.1529A>T
MANE Select
|
NP_004159.2:p.Glu510Val
|
|
NM_001294332.2:c.1385A>T
|
NP_001281261.1:p.Glu462Val
|
|
NM_001330758.2:c.1529A>T
|
NP_001317687.1:p.Glu510Val
|
|