ENST00000449291.7:c.1591A>C
MANE Select
|
ENSP00000401508.2:p.Ser531Arg
|
|
ENST00000340490.7:c.1676A>C
|
ENSP00000341136.3:p.Gln559Pro
|
|
ENST00000426292.7:c.1552A>C
|
ENSP00000390949.3:p.Ser518Arg
|
|
ENST00000435154.7:c.*300A>C
|
ENSP00000405670.3:n.*300A>C
|
|
ENST00000449291.6:c.1591A>C
|
ENSP00000401508.2:p.Ser531Arg
|
|
ENST00000460623.5:c.615A>C
|
|
|
ENST00000464332.5:n.1135A>C
|
|
|
ENST00000498076.5:n.370A>C
|
|
|
ENST00000529179.1:n.375A>C
|
|
|
NM_001286829.1:c.1552A>C
|
NP_001273758.1:p.Ser518Arg
|
|
NM_145201.5:c.1591A>C
|
NP_660202.3:p.Ser531Arg
|
|
XM_011517377.1:c.1328A>C
|
XP_011515679.1:p.Gln443Pro
|
|
NM_001363145.1:c.1510A>C
|
NP_001350074.1:p.Ser504Arg
|
|
NM_001363146.1:c.907A>C
|
NP_001350075.1:p.Ser303Arg
|
|
XM_017013975.2:c.1895A>C
|
XP_016869464.1:p.Gln632Pro
|
|
XM_017013976.2:c.1810A>C
|
XP_016869465.1:p.Ser604Arg
|
|
XM_017013977.2:c.1595A>C
|
XP_016869466.1:p.Gln532Pro
|
|
XM_017013978.2:c.1547A>C
|
XP_016869467.1:p.Gln516Pro
|
|
XM_017013979.2:c.992A>C
|
XP_016869468.1:p.Gln331Pro
|
|
XM_024447332.1:c.965A>C
|
XP_024303100.1:p.Gln322Pro
|
|
XM_024447333.1:c.911A>C
|
XP_024303101.1:p.Gln304Pro
|
|
NM_145201.6:c.1591A>C
MANE Select
|
NP_660202.3:p.Ser531Arg
|
|
NM_001286829.2:c.1552A>C
|
NP_001273758.1:p.Ser518Arg
|
|