ENST00000356141.9:c.1755C>T
MANE Select
|
ENSP00000348460.4:p.Ser585=
|
|
ENST00000551634.6:c.1764C>T
|
ENSP00000448373.2:p.Ser588=
|
|
ENST00000680362.1:c.1655C>T
|
|
|
ENST00000681323.1:c.793+2481C>T
|
|
|
ENST00000346562.6:c.1659C>T
|
ENSP00000319610.5:p.Ser553=
|
|
ENST00000356141.8:c.1755C>T
|
ENSP00000348460.4:p.Ser585=
|
|
ENST00000357798.9:c.1716C>T
|
ENSP00000350446.5:p.Ser572=
|
|
ENST00000548645.5:c.1665C>T
|
ENSP00000448916.1:p.Ser555=
|
|
ENST00000551492.5:c.1770C>T
|
ENSP00000450392.1:p.Ser590=
|
|
ENST00000551634.5:c.1677C>T
|
ENSP00000448373.1:p.Ser559=
|
|
NM_001164749.1:c.1755C>T
|
NP_001158221.1:p.Ser585=
|
|
NM_001165893.1:c.1665C>T
|
NP_001159365.1:p.Ser555=
|
|
NM_022123.2:c.1659C>T
|
NP_071406.1:p.Ser553=
|
|
NM_173159.2:c.1716C>T
|
NP_775182.1:p.Ser572=
|
|
XM_005267991.2:c.1776C>T
|
XP_005268048.1:p.Ser592=
|
|
XM_005267992.2:c.1770C>T
|
XP_005268049.1:p.Ser590=
|
|
XM_005267993.2:c.1716C>T
|
XP_005268050.1:p.Ser572=
|
|
XM_011537067.1:c.1806C>T
|
XP_011535369.1:p.Ser602=
|
|
XM_011537068.1:c.1797C>T
|
XP_011535370.1:p.Ser599=
|
|
XM_011537069.1:c.1767C>T
|
XP_011535371.1:p.Ser589=
|
|
XM_011537070.1:c.1710C>T
|
XP_011535372.1:p.Ser570=
|
|
XM_011537071.1:c.1677C>T
|
XP_011535373.1:p.Ser559=
|
|
XM_011537072.1:c.1656C>T
|
XP_011535374.1:p.Ser552=
|
|
XM_011537073.1:c.1449C>T
|
XP_011535375.1:p.Ser483=
|
|
XM_011537074.1:c.1449C>T
|
XP_011535376.1:p.Ser483=
|
|
XM_005267991.3:c.1863C>T
|
XP_005268048.2:p.Ser621=
|
|
XM_005267992.3:c.1857C>T
|
XP_005268049.2:p.Ser619=
|
|
XM_011537067.2:c.1806C>T
|
XP_011535369.1:p.Ser602=
|
|
XM_011537069.2:c.1854C>T
|
XP_011535371.2:p.Ser618=
|
|
XM_011537070.2:c.1710C>T
|
XP_011535372.1:p.Ser570=
|
|
XM_011537071.2:c.1764C>T
|
XP_011535373.2:p.Ser588=
|
|
XM_011537072.2:c.1656C>T
|
XP_011535374.1:p.Ser552=
|
|
XM_017021582.1:c.1914C>T
|
XP_016877071.1:p.Ser638=
|
|
XM_017021583.1:c.1905C>T
|
XP_016877072.1:p.Ser635=
|
|
XM_017021584.1:c.1824C>T
|
XP_016877073.1:p.Ser608=
|
|
XM_017021585.1:c.1773C>T
|
XP_016877074.1:p.Ser591=
|
|
XM_017021586.1:c.1449C>T
|
XP_016877075.1:p.Ser483=
|
|
XM_017021587.1:c.1449C>T
|
XP_016877076.1:p.Ser483=
|
|
XM_017021588.1:c.1449C>T
|
XP_016877077.1:p.Ser483=
|
|
NM_001164749.2:c.1755C>T
MANE Select
|
NP_001158221.1:p.Ser585=
|
|
NM_001165893.2:c.1665C>T
|
NP_001159365.1:p.Ser555=
|
|
NM_022123.3:c.1659C>T
|
NP_071406.1:p.Ser553=
|
|
NM_173159.3:c.1716C>T
|
NP_775182.1:p.Ser572=
|
|
NM_001394988.1:c.1710C>T
|
NP_001381917.1:p.Ser570=
|
|
NM_001394989.1:c.1656C>T
|
NP_001381918.1:p.Ser552=
|
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