ENST00000449291.7:c.1563G>A
MANE Select
|
ENSP00000401508.2:p.Leu521=
|
|
ENST00000340490.7:c.1648G>A
|
ENSP00000341136.3:p.Val550Ile
|
|
ENST00000426292.7:c.1524G>A
|
ENSP00000390949.3:p.Leu508=
|
|
ENST00000435154.7:c.*272G>A
|
ENSP00000405670.3:n.*272G>A
|
|
ENST00000449291.6:c.1563G>A
|
ENSP00000401508.2:p.Leu521=
|
|
ENST00000460623.5:c.587G>A
|
|
|
ENST00000464332.5:n.1107G>A
|
|
|
ENST00000498076.5:n.342G>A
|
|
|
ENST00000529179.1:n.347G>A
|
|
|
NM_001286829.1:c.1524G>A
|
NP_001273758.1:p.Leu508=
|
|
NM_145201.5:c.1563G>A
|
NP_660202.3:p.Leu521=
|
|
XM_011517377.1:c.1300G>A
|
XP_011515679.1:p.Val434Ile
|
|
NM_001363145.1:c.1482G>A
|
NP_001350074.1:p.Leu494=
|
|
NM_001363146.1:c.879G>A
|
NP_001350075.1:p.Leu293=
|
|
XM_017013975.2:c.1867G>A
|
XP_016869464.1:p.Val623Ile
|
|
XM_017013976.2:c.1782G>A
|
XP_016869465.1:p.Leu594=
|
|
XM_017013977.2:c.1567G>A
|
XP_016869466.1:p.Val523Ile
|
|
XM_017013978.2:c.1519G>A
|
XP_016869467.1:p.Val507Ile
|
|
XM_017013979.2:c.964G>A
|
XP_016869468.1:p.Val322Ile
|
|
XM_024447332.1:c.937G>A
|
XP_024303100.1:p.Val313Ile
|
|
XM_024447333.1:c.883G>A
|
XP_024303101.1:p.Val295Ile
|
|
NM_145201.6:c.1563G>A
MANE Select
|
NP_660202.3:p.Leu521=
|
|
NM_001286829.2:c.1524G>A
|
NP_001273758.1:p.Leu508=
|
|