ENST00000449291.7:c.1570A>T
MANE Select
|
ENSP00000401508.2:p.Arg524Trp
|
|
ENST00000340490.7:c.1655A>T
|
ENSP00000341136.3:p.Glu552Val
|
|
ENST00000426292.7:c.1531A>T
|
ENSP00000390949.3:p.Arg511Trp
|
|
ENST00000435154.7:c.*279A>T
|
ENSP00000405670.3:n.*279A>T
|
|
ENST00000449291.6:c.1570A>T
|
ENSP00000401508.2:p.Arg524Trp
|
|
ENST00000460623.5:c.594A>T
|
|
|
ENST00000464332.5:n.1114A>T
|
|
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ENST00000498076.5:n.349A>T
|
|
|
ENST00000529179.1:n.354A>T
|
|
|
NM_001286829.1:c.1531A>T
|
NP_001273758.1:p.Arg511Trp
|
|
NM_145201.5:c.1570A>T
|
NP_660202.3:p.Arg524Trp
|
|
XM_011517377.1:c.1307A>T
|
XP_011515679.1:p.Glu436Val
|
|
NM_001363145.1:c.1489A>T
|
NP_001350074.1:p.Arg497Trp
|
|
NM_001363146.1:c.886A>T
|
NP_001350075.1:p.Arg296Trp
|
|
XM_017013975.2:c.1874A>T
|
XP_016869464.1:p.Glu625Val
|
|
XM_017013976.2:c.1789A>T
|
XP_016869465.1:p.Arg597Trp
|
|
XM_017013977.2:c.1574A>T
|
XP_016869466.1:p.Glu525Val
|
|
XM_017013978.2:c.1526A>T
|
XP_016869467.1:p.Glu509Val
|
|
XM_017013979.2:c.971A>T
|
XP_016869468.1:p.Glu324Val
|
|
XM_024447332.1:c.944A>T
|
XP_024303100.1:p.Glu315Val
|
|
XM_024447333.1:c.890A>T
|
XP_024303101.1:p.Glu297Val
|
|
NM_145201.6:c.1570A>T
MANE Select
|
NP_660202.3:p.Arg524Trp
|
|
NM_001286829.2:c.1531A>T
|
NP_001273758.1:p.Arg511Trp
|
|