ENST00000449291.7:c.1587G>T
MANE Select
|
ENSP00000401508.2:p.Val529=
|
|
ENST00000340490.7:c.1672G>T
|
ENSP00000341136.3:p.Glu558Ter
|
|
ENST00000426292.7:c.1548G>T
|
ENSP00000390949.3:p.Val516=
|
|
ENST00000435154.7:c.*296G>T
|
ENSP00000405670.3:n.*296G>T
|
|
ENST00000449291.6:c.1587G>T
|
ENSP00000401508.2:p.Val529=
|
|
ENST00000460623.5:c.611G>T
|
|
|
ENST00000464332.5:n.1131G>T
|
|
|
ENST00000498076.5:n.366G>T
|
|
|
ENST00000529179.1:n.371G>T
|
|
|
NM_001286829.1:c.1548G>T
|
NP_001273758.1:p.Val516=
|
|
NM_145201.5:c.1587G>T
|
NP_660202.3:p.Val529=
|
|
XM_011517377.1:c.1324G>T
|
XP_011515679.1:p.Glu442Ter
|
|
NM_001363145.1:c.1506G>T
|
NP_001350074.1:p.Val502=
|
|
NM_001363146.1:c.903G>T
|
NP_001350075.1:p.Val301=
|
|
XM_017013975.2:c.1891G>T
|
XP_016869464.1:p.Glu631Ter
|
|
XM_017013976.2:c.1806G>T
|
XP_016869465.1:p.Val602=
|
|
XM_017013977.2:c.1591G>T
|
XP_016869466.1:p.Glu531Ter
|
|
XM_017013978.2:c.1543G>T
|
XP_016869467.1:p.Glu515Ter
|
|
XM_017013979.2:c.988G>T
|
XP_016869468.1:p.Glu330Ter
|
|
XM_024447332.1:c.961G>T
|
XP_024303100.1:p.Glu321Ter
|
|
XM_024447333.1:c.907G>T
|
XP_024303101.1:p.Glu303Ter
|
|
NM_145201.6:c.1587G>T
MANE Select
|
NP_660202.3:p.Val529=
|
|
NM_001286829.2:c.1548G>T
|
NP_001273758.1:p.Val516=
|
|