ENST00000449291.7:c.1595T>G
MANE Select
|
ENSP00000401508.2:p.Leu532Arg
|
|
ENST00000340490.7:c.1680T>G
|
ENSP00000341136.3:p.Ser560=
|
|
ENST00000426292.7:c.1556T>G
|
ENSP00000390949.3:p.Leu519Arg
|
|
ENST00000435154.7:c.*304T>G
|
ENSP00000405670.3:n.*304T>G
|
|
ENST00000449291.6:c.1595T>G
|
ENSP00000401508.2:p.Leu532Arg
|
|
ENST00000460623.5:c.619T>G
|
|
|
ENST00000464332.5:n.1139T>G
|
|
|
ENST00000498076.5:n.374T>G
|
|
|
ENST00000529179.1:n.379T>G
|
|
|
NM_001286829.1:c.1556T>G
|
NP_001273758.1:p.Leu519Arg
|
|
NM_145201.5:c.1595T>G
|
NP_660202.3:p.Leu532Arg
|
|
XM_011517377.1:c.1332T>G
|
XP_011515679.1:p.Ser444=
|
|
NM_001363145.1:c.1514T>G
|
NP_001350074.1:p.Leu505Arg
|
|
NM_001363146.1:c.911T>G
|
NP_001350075.1:p.Leu304Arg
|
|
XM_017013975.2:c.1899T>G
|
XP_016869464.1:p.Ser633=
|
|
XM_017013976.2:c.1814T>G
|
XP_016869465.1:p.Leu605Arg
|
|
XM_017013977.2:c.1599T>G
|
XP_016869466.1:p.Ser533=
|
|
XM_017013978.2:c.1551T>G
|
XP_016869467.1:p.Ser517=
|
|
XM_017013979.2:c.996T>G
|
XP_016869468.1:p.Ser332=
|
|
XM_024447332.1:c.969T>G
|
XP_024303100.1:p.Ser323=
|
|
XM_024447333.1:c.915T>G
|
XP_024303101.1:p.Ser305=
|
|
NM_145201.6:c.1595T>G
MANE Select
|
NP_660202.3:p.Leu532Arg
|
|
NM_001286829.2:c.1556T>G
|
NP_001273758.1:p.Leu519Arg
|
|