ENST00000449291.7:c.1580C>T
MANE Select
|
ENSP00000401508.2:p.Ala527Val
|
|
ENST00000340490.7:c.1665C>T
|
ENSP00000341136.3:p.Gly555=
|
|
ENST00000426292.7:c.1541C>T
|
ENSP00000390949.3:p.Ala514Val
|
|
ENST00000435154.7:c.*289C>T
|
ENSP00000405670.3:n.*289C>T
|
|
ENST00000449291.6:c.1580C>T
|
ENSP00000401508.2:p.Ala527Val
|
|
ENST00000460623.5:c.604C>T
|
|
|
ENST00000464332.5:n.1124C>T
|
|
|
ENST00000498076.5:n.359C>T
|
|
|
ENST00000529179.1:n.364C>T
|
|
|
NM_001286829.1:c.1541C>T
|
NP_001273758.1:p.Ala514Val
|
|
NM_145201.5:c.1580C>T
|
NP_660202.3:p.Ala527Val
|
|
XM_011517377.1:c.1317C>T
|
XP_011515679.1:p.Gly439=
|
|
NM_001363145.1:c.1499C>T
|
NP_001350074.1:p.Ala500Val
|
|
NM_001363146.1:c.896C>T
|
NP_001350075.1:p.Ala299Val
|
|
XM_017013975.2:c.1884C>T
|
XP_016869464.1:p.Gly628=
|
|
XM_017013976.2:c.1799C>T
|
XP_016869465.1:p.Ala600Val
|
|
XM_017013977.2:c.1584C>T
|
XP_016869466.1:p.Gly528=
|
|
XM_017013978.2:c.1536C>T
|
XP_016869467.1:p.Gly512=
|
|
XM_017013979.2:c.981C>T
|
XP_016869468.1:p.Gly327=
|
|
XM_024447332.1:c.954C>T
|
XP_024303100.1:p.Gly318=
|
|
XM_024447333.1:c.900C>T
|
XP_024303101.1:p.Gly300=
|
|
NM_145201.6:c.1580C>T
MANE Select
|
NP_660202.3:p.Ala527Val
|
|
NM_001286829.2:c.1541C>T
|
NP_001273758.1:p.Ala514Val
|
|