ENST00000356141.9:c.1908G>A
MANE Select
|
ENSP00000348460.4:p.Leu636=
|
|
ENST00000551634.6:c.1917G>A
|
ENSP00000448373.2:p.Leu639=
|
|
ENST00000680362.1:c.1808G>A
|
|
|
ENST00000681323.1:c.793+2634G>A
|
|
|
ENST00000346562.6:c.1812G>A
|
ENSP00000319610.5:p.Leu604=
|
|
ENST00000356141.8:c.1908G>A
|
ENSP00000348460.4:p.Leu636=
|
|
ENST00000357798.9:c.1869G>A
|
ENSP00000350446.5:p.Leu623=
|
|
ENST00000548645.5:c.1818G>A
|
ENSP00000448916.1:p.Leu606=
|
|
ENST00000551492.5:c.1923G>A
|
ENSP00000450392.1:p.Leu641=
|
|
ENST00000551634.5:c.1830G>A
|
ENSP00000448373.1:p.Leu610=
|
|
NM_001164749.1:c.1908G>A
|
NP_001158221.1:p.Leu636=
|
|
NM_001165893.1:c.1818G>A
|
NP_001159365.1:p.Leu606=
|
|
NM_022123.2:c.1812G>A
|
NP_071406.1:p.Leu604=
|
|
NM_173159.2:c.1869G>A
|
NP_775182.1:p.Leu623=
|
|
XM_005267991.2:c.1929G>A
|
XP_005268048.1:p.Leu643=
|
|
XM_005267992.2:c.1923G>A
|
XP_005268049.1:p.Leu641=
|
|
XM_005267993.2:c.1869G>A
|
XP_005268050.1:p.Leu623=
|
|
XM_011537067.1:c.1959G>A
|
XP_011535369.1:p.Leu653=
|
|
XM_011537068.1:c.1950G>A
|
XP_011535370.1:p.Leu650=
|
|
XM_011537069.1:c.1920G>A
|
XP_011535371.1:p.Leu640=
|
|
XM_011537070.1:c.1863G>A
|
XP_011535372.1:p.Leu621=
|
|
XM_011537071.1:c.1830G>A
|
XP_011535373.1:p.Leu610=
|
|
XM_011537072.1:c.1809G>A
|
XP_011535374.1:p.Leu603=
|
|
XM_011537073.1:c.1602G>A
|
XP_011535375.1:p.Leu534=
|
|
XM_011537074.1:c.1602G>A
|
XP_011535376.1:p.Leu534=
|
|
XM_005267991.3:c.2016G>A
|
XP_005268048.2:p.Leu672=
|
|
XM_005267992.3:c.2010G>A
|
XP_005268049.2:p.Leu670=
|
|
XM_011537067.2:c.1959G>A
|
XP_011535369.1:p.Leu653=
|
|
XM_011537069.2:c.2007G>A
|
XP_011535371.2:p.Leu669=
|
|
XM_011537070.2:c.1863G>A
|
XP_011535372.1:p.Leu621=
|
|
XM_011537071.2:c.1917G>A
|
XP_011535373.2:p.Leu639=
|
|
XM_011537072.2:c.1809G>A
|
XP_011535374.1:p.Leu603=
|
|
XM_017021582.1:c.2067G>A
|
XP_016877071.1:p.Leu689=
|
|
XM_017021583.1:c.2058G>A
|
XP_016877072.1:p.Leu686=
|
|
XM_017021584.1:c.1977G>A
|
XP_016877073.1:p.Leu659=
|
|
XM_017021585.1:c.1926G>A
|
XP_016877074.1:p.Leu642=
|
|
XM_017021586.1:c.1602G>A
|
XP_016877075.1:p.Leu534=
|
|
XM_017021587.1:c.1602G>A
|
XP_016877076.1:p.Leu534=
|
|
XM_017021588.1:c.1602G>A
|
XP_016877077.1:p.Leu534=
|
|
NM_001164749.2:c.1908G>A
MANE Select
|
NP_001158221.1:p.Leu636=
|
|
NM_001165893.2:c.1818G>A
|
NP_001159365.1:p.Leu606=
|
|
NM_022123.3:c.1812G>A
|
NP_071406.1:p.Leu604=
|
|
NM_173159.3:c.1869G>A
|
NP_775182.1:p.Leu623=
|
|
NM_001394988.1:c.1863G>A
|
NP_001381917.1:p.Leu621=
|
|
NM_001394989.1:c.1809G>A
|
NP_001381918.1:p.Leu603=
|
|