ENST00000449291.7:c.1507C>A
MANE Select
|
ENSP00000401508.2:p.Arg503=
|
|
ENST00000340490.7:c.1507C>A
|
ENSP00000341136.3:p.Arg503=
|
|
ENST00000426292.7:c.1468C>A
|
ENSP00000390949.3:p.Arg490=
|
|
ENST00000435154.7:c.*131C>A
|
ENSP00000405670.3:n.*131C>A
|
|
ENST00000449291.6:c.1507C>A
|
ENSP00000401508.2:p.Arg503=
|
|
ENST00000460623.5:c.446C>A
|
|
|
ENST00000464332.5:n.1051C>A
|
|
|
ENST00000498076.5:n.286C>A
|
|
|
ENST00000529179.1:n.291C>A
|
|
|
NM_001286829.1:c.1468C>A
|
NP_001273758.1:p.Arg490=
|
|
NM_145201.5:c.1507C>A
|
NP_660202.3:p.Arg503=
|
|
XM_011517377.1:c.1292-133C>A
|
XP_011515679.1:n.1292-133C>A
|
|
NM_001363145.1:c.1426C>A
|
NP_001350074.1:p.Arg476=
|
|
NM_001363146.1:c.823C>A
|
NP_001350075.1:p.Arg275=
|
|
XM_017013975.2:c.1726C>A
|
XP_016869464.1:p.Arg576=
|
|
XM_017013976.2:c.1726C>A
|
XP_016869465.1:p.Arg576=
|
|
XM_017013977.2:c.1426C>A
|
XP_016869466.1:p.Arg476=
|
|
XM_017013978.2:c.1511-133C>A
|
XP_016869467.1:n.1511-133C>A
|
|
XM_017013979.2:c.823C>A
|
XP_016869468.1:p.Arg275=
|
|
XM_024447332.1:c.929-133C>A
|
XP_024303100.1:n.929-133C>A
|
|
XM_024447333.1:c.742C>A
|
XP_024303101.1:p.Arg248=
|
|
NM_145201.6:c.1507C>A
MANE Select
|
NP_660202.3:p.Arg503=
|
|
NM_001286829.2:c.1468C>A
|
NP_001273758.1:p.Arg490=
|
|