ENST00000356141.9:c.1751A>T
MANE Select
|
ENSP00000348460.4:p.Asp584Val
|
|
ENST00000551634.6:c.1760A>T
|
ENSP00000448373.2:p.Asp587Val
|
|
ENST00000680362.1:c.1651A>T
|
|
|
ENST00000681323.1:c.793+2477A>T
|
|
|
ENST00000346562.6:c.1655A>T
|
ENSP00000319610.5:p.Asp552Val
|
|
ENST00000356141.8:c.1751A>T
|
ENSP00000348460.4:p.Asp584Val
|
|
ENST00000357798.9:c.1712A>T
|
ENSP00000350446.5:p.Asp571Val
|
|
ENST00000548645.5:c.1661A>T
|
ENSP00000448916.1:p.Asp554Val
|
|
ENST00000551492.5:c.1766A>T
|
ENSP00000450392.1:p.Asp589Val
|
|
ENST00000551634.5:c.1673A>T
|
ENSP00000448373.1:p.Asp558Val
|
|
NM_001164749.1:c.1751A>T
|
NP_001158221.1:p.Asp584Val
|
|
NM_001165893.1:c.1661A>T
|
NP_001159365.1:p.Asp554Val
|
|
NM_022123.2:c.1655A>T
|
NP_071406.1:p.Asp552Val
|
|
NM_173159.2:c.1712A>T
|
NP_775182.1:p.Asp571Val
|
|
XM_005267991.2:c.1772A>T
|
XP_005268048.1:p.Asp591Val
|
|
XM_005267992.2:c.1766A>T
|
XP_005268049.1:p.Asp589Val
|
|
XM_005267993.2:c.1712A>T
|
XP_005268050.1:p.Asp571Val
|
|
XM_011537067.1:c.1802A>T
|
XP_011535369.1:p.Asp601Val
|
|
XM_011537068.1:c.1793A>T
|
XP_011535370.1:p.Asp598Val
|
|
XM_011537069.1:c.1763A>T
|
XP_011535371.1:p.Asp588Val
|
|
XM_011537070.1:c.1706A>T
|
XP_011535372.1:p.Asp569Val
|
|
XM_011537071.1:c.1673A>T
|
XP_011535373.1:p.Asp558Val
|
|
XM_011537072.1:c.1652A>T
|
XP_011535374.1:p.Asp551Val
|
|
XM_011537073.1:c.1445A>T
|
XP_011535375.1:p.Asp482Val
|
|
XM_011537074.1:c.1445A>T
|
XP_011535376.1:p.Asp482Val
|
|
XM_005267991.3:c.1859A>T
|
XP_005268048.2:p.Asp620Val
|
|
XM_005267992.3:c.1853A>T
|
XP_005268049.2:p.Asp618Val
|
|
XM_011537067.2:c.1802A>T
|
XP_011535369.1:p.Asp601Val
|
|
XM_011537069.2:c.1850A>T
|
XP_011535371.2:p.Asp617Val
|
|
XM_011537070.2:c.1706A>T
|
XP_011535372.1:p.Asp569Val
|
|
XM_011537071.2:c.1760A>T
|
XP_011535373.2:p.Asp587Val
|
|
XM_011537072.2:c.1652A>T
|
XP_011535374.1:p.Asp551Val
|
|
XM_017021582.1:c.1910A>T
|
XP_016877071.1:p.Asp637Val
|
|
XM_017021583.1:c.1901A>T
|
XP_016877072.1:p.Asp634Val
|
|
XM_017021584.1:c.1820A>T
|
XP_016877073.1:p.Asp607Val
|
|
XM_017021585.1:c.1769A>T
|
XP_016877074.1:p.Asp590Val
|
|
XM_017021586.1:c.1445A>T
|
XP_016877075.1:p.Asp482Val
|
|
XM_017021587.1:c.1445A>T
|
XP_016877076.1:p.Asp482Val
|
|
XM_017021588.1:c.1445A>T
|
XP_016877077.1:p.Asp482Val
|
|
NM_001164749.2:c.1751A>T
MANE Select
|
NP_001158221.1:p.Asp584Val
|
|
NM_001165893.2:c.1661A>T
|
NP_001159365.1:p.Asp554Val
|
|
NM_022123.3:c.1655A>T
|
NP_071406.1:p.Asp552Val
|
|
NM_173159.3:c.1712A>T
|
NP_775182.1:p.Asp571Val
|
|
NM_001394988.1:c.1706A>T
|
NP_001381917.1:p.Asp569Val
|
|
NM_001394989.1:c.1652A>T
|
NP_001381918.1:p.Asp551Val
|
|