ENST00000449291.7:c.1565C>G
MANE Select
|
ENSP00000401508.2:p.Ser522Cys
|
|
ENST00000340490.7:c.1650C>G
|
ENSP00000341136.3:p.Val550=
|
|
ENST00000426292.7:c.1526C>G
|
ENSP00000390949.3:p.Ser509Cys
|
|
ENST00000435154.7:c.*274C>G
|
ENSP00000405670.3:n.*274C>G
|
|
ENST00000449291.6:c.1565C>G
|
ENSP00000401508.2:p.Ser522Cys
|
|
ENST00000460623.5:c.589C>G
|
|
|
ENST00000464332.5:n.1109C>G
|
|
|
ENST00000498076.5:n.344C>G
|
|
|
ENST00000529179.1:n.349C>G
|
|
|
NM_001286829.1:c.1526C>G
|
NP_001273758.1:p.Ser509Cys
|
|
NM_145201.5:c.1565C>G
|
NP_660202.3:p.Ser522Cys
|
|
XM_011517377.1:c.1302C>G
|
XP_011515679.1:p.Val434=
|
|
NM_001363145.1:c.1484C>G
|
NP_001350074.1:p.Ser495Cys
|
|
NM_001363146.1:c.881C>G
|
NP_001350075.1:p.Ser294Cys
|
|
XM_017013975.2:c.1869C>G
|
XP_016869464.1:p.Val623=
|
|
XM_017013976.2:c.1784C>G
|
XP_016869465.1:p.Ser595Cys
|
|
XM_017013977.2:c.1569C>G
|
XP_016869466.1:p.Val523=
|
|
XM_017013978.2:c.1521C>G
|
XP_016869467.1:p.Val507=
|
|
XM_017013979.2:c.966C>G
|
XP_016869468.1:p.Val322=
|
|
XM_024447332.1:c.939C>G
|
XP_024303100.1:p.Val313=
|
|
XM_024447333.1:c.885C>G
|
XP_024303101.1:p.Val295=
|
|
NM_145201.6:c.1565C>G
MANE Select
|
NP_660202.3:p.Ser522Cys
|
|
NM_001286829.2:c.1526C>G
|
NP_001273758.1:p.Ser509Cys
|
|