ENST00000356141.9:c.1745A>T
MANE Select
|
ENSP00000348460.4:p.Asp582Val
|
|
ENST00000551634.6:c.1754A>T
|
ENSP00000448373.2:p.Asp585Val
|
|
ENST00000680362.1:c.1645A>T
|
|
|
ENST00000681323.1:c.793+2471A>T
|
|
|
ENST00000346562.6:c.1649A>T
|
ENSP00000319610.5:p.Asp550Val
|
|
ENST00000356141.8:c.1745A>T
|
ENSP00000348460.4:p.Asp582Val
|
|
ENST00000357798.9:c.1706A>T
|
ENSP00000350446.5:p.Asp569Val
|
|
ENST00000548645.5:c.1655A>T
|
ENSP00000448916.1:p.Asp552Val
|
|
ENST00000551492.5:c.1760A>T
|
ENSP00000450392.1:p.Asp587Val
|
|
ENST00000551634.5:c.1667A>T
|
ENSP00000448373.1:p.Asp556Val
|
|
NM_001164749.1:c.1745A>T
|
NP_001158221.1:p.Asp582Val
|
|
NM_001165893.1:c.1655A>T
|
NP_001159365.1:p.Asp552Val
|
|
NM_022123.2:c.1649A>T
|
NP_071406.1:p.Asp550Val
|
|
NM_173159.2:c.1706A>T
|
NP_775182.1:p.Asp569Val
|
|
XM_005267991.2:c.1766A>T
|
XP_005268048.1:p.Asp589Val
|
|
XM_005267992.2:c.1760A>T
|
XP_005268049.1:p.Asp587Val
|
|
XM_005267993.2:c.1706A>T
|
XP_005268050.1:p.Asp569Val
|
|
XM_011537067.1:c.1796A>T
|
XP_011535369.1:p.Asp599Val
|
|
XM_011537068.1:c.1787A>T
|
XP_011535370.1:p.Asp596Val
|
|
XM_011537069.1:c.1757A>T
|
XP_011535371.1:p.Asp586Val
|
|
XM_011537070.1:c.1700A>T
|
XP_011535372.1:p.Asp567Val
|
|
XM_011537071.1:c.1667A>T
|
XP_011535373.1:p.Asp556Val
|
|
XM_011537072.1:c.1646A>T
|
XP_011535374.1:p.Asp549Val
|
|
XM_011537073.1:c.1439A>T
|
XP_011535375.1:p.Asp480Val
|
|
XM_011537074.1:c.1439A>T
|
XP_011535376.1:p.Asp480Val
|
|
XM_005267991.3:c.1853A>T
|
XP_005268048.2:p.Asp618Val
|
|
XM_005267992.3:c.1847A>T
|
XP_005268049.2:p.Asp616Val
|
|
XM_011537067.2:c.1796A>T
|
XP_011535369.1:p.Asp599Val
|
|
XM_011537069.2:c.1844A>T
|
XP_011535371.2:p.Asp615Val
|
|
XM_011537070.2:c.1700A>T
|
XP_011535372.1:p.Asp567Val
|
|
XM_011537071.2:c.1754A>T
|
XP_011535373.2:p.Asp585Val
|
|
XM_011537072.2:c.1646A>T
|
XP_011535374.1:p.Asp549Val
|
|
XM_017021582.1:c.1904A>T
|
XP_016877071.1:p.Asp635Val
|
|
XM_017021583.1:c.1895A>T
|
XP_016877072.1:p.Asp632Val
|
|
XM_017021584.1:c.1814A>T
|
XP_016877073.1:p.Asp605Val
|
|
XM_017021585.1:c.1763A>T
|
XP_016877074.1:p.Asp588Val
|
|
XM_017021586.1:c.1439A>T
|
XP_016877075.1:p.Asp480Val
|
|
XM_017021587.1:c.1439A>T
|
XP_016877076.1:p.Asp480Val
|
|
XM_017021588.1:c.1439A>T
|
XP_016877077.1:p.Asp480Val
|
|
NM_001164749.2:c.1745A>T
MANE Select
|
NP_001158221.1:p.Asp582Val
|
|
NM_001165893.2:c.1655A>T
|
NP_001159365.1:p.Asp552Val
|
|
NM_022123.3:c.1649A>T
|
NP_071406.1:p.Asp550Val
|
|
NM_173159.3:c.1706A>T
|
NP_775182.1:p.Asp569Val
|
|
NM_001394988.1:c.1700A>T
|
NP_001381917.1:p.Asp567Val
|
|
NM_001394989.1:c.1646A>T
|
NP_001381918.1:p.Asp549Val
|
|