ENST00000449291.7:c.1557G>T
MANE Select
|
ENSP00000401508.2:p.Val519=
|
|
ENST00000340490.7:c.1642G>T
|
ENSP00000341136.3:p.Gly548Cys
|
|
ENST00000426292.7:c.1518G>T
|
ENSP00000390949.3:p.Val506=
|
|
ENST00000435154.7:c.*266G>T
|
ENSP00000405670.3:n.*266G>T
|
|
ENST00000449291.6:c.1557G>T
|
ENSP00000401508.2:p.Val519=
|
|
ENST00000460623.5:c.581G>T
|
|
|
ENST00000464332.5:n.1101G>T
|
|
|
ENST00000498076.5:n.336G>T
|
|
|
ENST00000529179.1:n.341G>T
|
|
|
NM_001286829.1:c.1518G>T
|
NP_001273758.1:p.Val506=
|
|
NM_145201.5:c.1557G>T
|
NP_660202.3:p.Val519=
|
|
XM_011517377.1:c.1294G>T
|
XP_011515679.1:p.Gly432Cys
|
|
NM_001363145.1:c.1476G>T
|
NP_001350074.1:p.Val492=
|
|
NM_001363146.1:c.873G>T
|
NP_001350075.1:p.Val291=
|
|
XM_017013975.2:c.1861G>T
|
XP_016869464.1:p.Gly621Cys
|
|
XM_017013976.2:c.1776G>T
|
XP_016869465.1:p.Val592=
|
|
XM_017013977.2:c.1561G>T
|
XP_016869466.1:p.Gly521Cys
|
|
XM_017013978.2:c.1513G>T
|
XP_016869467.1:p.Gly505Cys
|
|
XM_017013979.2:c.958G>T
|
XP_016869468.1:p.Gly320Cys
|
|
XM_024447332.1:c.931G>T
|
XP_024303100.1:p.Gly311Cys
|
|
XM_024447333.1:c.877G>T
|
XP_024303101.1:p.Gly293Cys
|
|
NM_145201.6:c.1557G>T
MANE Select
|
NP_660202.3:p.Val519=
|
|
NM_001286829.2:c.1518G>T
|
NP_001273758.1:p.Val506=
|
|