ENST00000449291.7:c.1573C>T
MANE Select
|
ENSP00000401508.2:p.Leu525=
|
|
ENST00000340490.7:c.1658C>T
|
ENSP00000341136.3:p.Ala553Val
|
|
ENST00000426292.7:c.1534C>T
|
ENSP00000390949.3:p.Leu512=
|
|
ENST00000435154.7:c.*282C>T
|
ENSP00000405670.3:n.*282C>T
|
|
ENST00000449291.6:c.1573C>T
|
ENSP00000401508.2:p.Leu525=
|
|
ENST00000460623.5:c.597C>T
|
|
|
ENST00000464332.5:n.1117C>T
|
|
|
ENST00000498076.5:n.352C>T
|
|
|
ENST00000529179.1:n.357C>T
|
|
|
NM_001286829.1:c.1534C>T
|
NP_001273758.1:p.Leu512=
|
|
NM_145201.5:c.1573C>T
|
NP_660202.3:p.Leu525=
|
|
XM_011517377.1:c.1310C>T
|
XP_011515679.1:p.Ala437Val
|
|
NM_001363145.1:c.1492C>T
|
NP_001350074.1:p.Leu498=
|
|
NM_001363146.1:c.889C>T
|
NP_001350075.1:p.Leu297=
|
|
XM_017013975.2:c.1877C>T
|
XP_016869464.1:p.Ala626Val
|
|
XM_017013976.2:c.1792C>T
|
XP_016869465.1:p.Leu598=
|
|
XM_017013977.2:c.1577C>T
|
XP_016869466.1:p.Ala526Val
|
|
XM_017013978.2:c.1529C>T
|
XP_016869467.1:p.Ala510Val
|
|
XM_017013979.2:c.974C>T
|
XP_016869468.1:p.Ala325Val
|
|
XM_024447332.1:c.947C>T
|
XP_024303100.1:p.Ala316Val
|
|
XM_024447333.1:c.893C>T
|
XP_024303101.1:p.Ala298Val
|
|
NM_145201.6:c.1573C>T
MANE Select
|
NP_660202.3:p.Leu525=
|
|
NM_001286829.2:c.1534C>T
|
NP_001273758.1:p.Leu512=
|
|