ENST00000449291.7:c.1576C>T
MANE Select
|
ENSP00000401508.2:p.Gln526Ter
|
|
ENST00000340490.7:c.1661C>T
|
ENSP00000341136.3:p.Ala554Val
|
|
ENST00000426292.7:c.1537C>T
|
ENSP00000390949.3:p.Gln513Ter
|
|
ENST00000435154.7:c.*285C>T
|
ENSP00000405670.3:n.*285C>T
|
|
ENST00000449291.6:c.1576C>T
|
ENSP00000401508.2:p.Gln526Ter
|
|
ENST00000460623.5:c.600C>T
|
|
|
ENST00000464332.5:n.1120C>T
|
|
|
ENST00000498076.5:n.355C>T
|
|
|
ENST00000529179.1:n.360C>T
|
|
|
NM_001286829.1:c.1537C>T
|
NP_001273758.1:p.Gln513Ter
|
|
NM_145201.5:c.1576C>T
|
NP_660202.3:p.Gln526Ter
|
|
XM_011517377.1:c.1313C>T
|
XP_011515679.1:p.Ala438Val
|
|
NM_001363145.1:c.1495C>T
|
NP_001350074.1:p.Gln499Ter
|
|
NM_001363146.1:c.892C>T
|
NP_001350075.1:p.Gln298Ter
|
|
XM_017013975.2:c.1880C>T
|
XP_016869464.1:p.Ala627Val
|
|
XM_017013976.2:c.1795C>T
|
XP_016869465.1:p.Gln599Ter
|
|
XM_017013977.2:c.1580C>T
|
XP_016869466.1:p.Ala527Val
|
|
XM_017013978.2:c.1532C>T
|
XP_016869467.1:p.Ala511Val
|
|
XM_017013979.2:c.977C>T
|
XP_016869468.1:p.Ala326Val
|
|
XM_024447332.1:c.950C>T
|
XP_024303100.1:p.Ala317Val
|
|
XM_024447333.1:c.896C>T
|
XP_024303101.1:p.Ala299Val
|
|
NM_145201.6:c.1576C>T
MANE Select
|
NP_660202.3:p.Gln526Ter
|
|
NM_001286829.2:c.1537C>T
|
NP_001273758.1:p.Gln513Ter
|
|