ENST00000449291.7:c.1597T=
MANE Select
|
ENSP00000401508.2:p.Cys533=
|
|
ENST00000340490.7:c.1682T=
|
ENSP00000341136.3:p.Val561=
|
|
ENST00000426292.7:c.1558T=
|
ENSP00000390949.3:p.Cys520=
|
|
ENST00000435154.7:c.*306T=
|
ENSP00000405670.3:n.*306T=
|
|
ENST00000449291.6:c.1597T=
|
ENSP00000401508.2:p.Cys533=
|
|
ENST00000460623.5:c.621T=
|
|
|
ENST00000464332.5:n.1141T=
|
|
|
ENST00000498076.5:n.376T=
|
|
|
ENST00000529179.1:n.381T=
|
|
|
NM_001286829.1:c.1558T=
|
NP_001273758.1:p.Cys520=
|
|
NM_145201.5:c.1597T=
|
NP_660202.3:p.Cys533=
|
|
XM_011517377.1:c.1334T=
|
XP_011515679.1:p.Val445=
|
|
NM_001363145.1:c.1516T=
|
NP_001350074.1:p.Cys506=
|
|
NM_001363146.1:c.913T=
|
NP_001350075.1:p.Cys305=
|
|
XM_017013975.2:c.1901T=
|
XP_016869464.1:p.Val634=
|
|
XM_017013976.2:c.1816T=
|
XP_016869465.1:p.Cys606=
|
|
XM_017013977.2:c.1601T=
|
XP_016869466.1:p.Val534=
|
|
XM_017013978.2:c.1553T=
|
XP_016869467.1:p.Val518=
|
|
XM_017013979.2:c.998T=
|
XP_016869468.1:p.Val333=
|
|
XM_024447332.1:c.971T=
|
XP_024303100.1:p.Val324=
|
|
XM_024447333.1:c.917T=
|
XP_024303101.1:p.Val306=
|
|
NM_145201.6:c.1597T=
MANE Select
|
NP_660202.3:p.Cys533=
|
|
NM_001286829.2:c.1558T=
|
NP_001273758.1:p.Cys520=
|
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