ENST00000356141.9:c.1911G>A
MANE Select
|
ENSP00000348460.4:p.Leu637=
|
|
ENST00000551634.6:c.1920G>A
|
ENSP00000448373.2:p.Leu640=
|
|
ENST00000680362.1:c.1811G>A
|
|
|
ENST00000681323.1:c.793+2637G>A
|
|
|
ENST00000346562.6:c.1815G>A
|
ENSP00000319610.5:p.Leu605=
|
|
ENST00000356141.8:c.1911G>A
|
ENSP00000348460.4:p.Leu637=
|
|
ENST00000357798.9:c.1872G>A
|
ENSP00000350446.5:p.Leu624=
|
|
ENST00000548645.5:c.1821G>A
|
ENSP00000448916.1:p.Leu607=
|
|
ENST00000551492.5:c.1926G>A
|
ENSP00000450392.1:p.Leu642=
|
|
ENST00000551634.5:c.1833G>A
|
ENSP00000448373.1:p.Leu611=
|
|
NM_001164749.1:c.1911G>A
|
NP_001158221.1:p.Leu637=
|
|
NM_001165893.1:c.1821G>A
|
NP_001159365.1:p.Leu607=
|
|
NM_022123.2:c.1815G>A
|
NP_071406.1:p.Leu605=
|
|
NM_173159.2:c.1872G>A
|
NP_775182.1:p.Leu624=
|
|
XM_005267991.2:c.1932G>A
|
XP_005268048.1:p.Leu644=
|
|
XM_005267992.2:c.1926G>A
|
XP_005268049.1:p.Leu642=
|
|
XM_005267993.2:c.1872G>A
|
XP_005268050.1:p.Leu624=
|
|
XM_011537067.1:c.1962G>A
|
XP_011535369.1:p.Leu654=
|
|
XM_011537068.1:c.1953G>A
|
XP_011535370.1:p.Leu651=
|
|
XM_011537069.1:c.1923G>A
|
XP_011535371.1:p.Leu641=
|
|
XM_011537070.1:c.1866G>A
|
XP_011535372.1:p.Leu622=
|
|
XM_011537071.1:c.1833G>A
|
XP_011535373.1:p.Leu611=
|
|
XM_011537072.1:c.1812G>A
|
XP_011535374.1:p.Leu604=
|
|
XM_011537073.1:c.1605G>A
|
XP_011535375.1:p.Leu535=
|
|
XM_011537074.1:c.1605G>A
|
XP_011535376.1:p.Leu535=
|
|
XM_005267991.3:c.2019G>A
|
XP_005268048.2:p.Leu673=
|
|
XM_005267992.3:c.2013G>A
|
XP_005268049.2:p.Leu671=
|
|
XM_011537067.2:c.1962G>A
|
XP_011535369.1:p.Leu654=
|
|
XM_011537069.2:c.2010G>A
|
XP_011535371.2:p.Leu670=
|
|
XM_011537070.2:c.1866G>A
|
XP_011535372.1:p.Leu622=
|
|
XM_011537071.2:c.1920G>A
|
XP_011535373.2:p.Leu640=
|
|
XM_011537072.2:c.1812G>A
|
XP_011535374.1:p.Leu604=
|
|
XM_017021582.1:c.2070G>A
|
XP_016877071.1:p.Leu690=
|
|
XM_017021583.1:c.2061G>A
|
XP_016877072.1:p.Leu687=
|
|
XM_017021584.1:c.1980G>A
|
XP_016877073.1:p.Leu660=
|
|
XM_017021585.1:c.1929G>A
|
XP_016877074.1:p.Leu643=
|
|
XM_017021586.1:c.1605G>A
|
XP_016877075.1:p.Leu535=
|
|
XM_017021587.1:c.1605G>A
|
XP_016877076.1:p.Leu535=
|
|
XM_017021588.1:c.1605G>A
|
XP_016877077.1:p.Leu535=
|
|
NM_001164749.2:c.1911G>A
MANE Select
|
NP_001158221.1:p.Leu637=
|
|
NM_001165893.2:c.1821G>A
|
NP_001159365.1:p.Leu607=
|
|
NM_022123.3:c.1815G>A
|
NP_071406.1:p.Leu605=
|
|
NM_173159.3:c.1872G>A
|
NP_775182.1:p.Leu624=
|
|
NM_001394988.1:c.1866G>A
|
NP_001381917.1:p.Leu622=
|
|
NM_001394989.1:c.1812G>A
|
NP_001381918.1:p.Leu604=
|
|