ENST00000356141.9:c.1890G>T
MANE Select
|
ENSP00000348460.4:p.Leu630=
|
|
ENST00000551634.6:c.1899G>T
|
ENSP00000448373.2:p.Leu633=
|
|
ENST00000680362.1:c.1790G>T
|
|
|
ENST00000681323.1:c.793+2616G>T
|
|
|
ENST00000346562.6:c.1794G>T
|
ENSP00000319610.5:p.Leu598=
|
|
ENST00000356141.8:c.1890G>T
|
ENSP00000348460.4:p.Leu630=
|
|
ENST00000357798.9:c.1851G>T
|
ENSP00000350446.5:p.Leu617=
|
|
ENST00000548645.5:c.1800G>T
|
ENSP00000448916.1:p.Leu600=
|
|
ENST00000551492.5:c.1905G>T
|
ENSP00000450392.1:p.Leu635=
|
|
ENST00000551634.5:c.1812G>T
|
ENSP00000448373.1:p.Leu604=
|
|
NM_001164749.1:c.1890G>T
|
NP_001158221.1:p.Leu630=
|
|
NM_001165893.1:c.1800G>T
|
NP_001159365.1:p.Leu600=
|
|
NM_022123.2:c.1794G>T
|
NP_071406.1:p.Leu598=
|
|
NM_173159.2:c.1851G>T
|
NP_775182.1:p.Leu617=
|
|
XM_005267991.2:c.1911G>T
|
XP_005268048.1:p.Leu637=
|
|
XM_005267992.2:c.1905G>T
|
XP_005268049.1:p.Leu635=
|
|
XM_005267993.2:c.1851G>T
|
XP_005268050.1:p.Leu617=
|
|
XM_011537067.1:c.1941G>T
|
XP_011535369.1:p.Leu647=
|
|
XM_011537068.1:c.1932G>T
|
XP_011535370.1:p.Leu644=
|
|
XM_011537069.1:c.1902G>T
|
XP_011535371.1:p.Leu634=
|
|
XM_011537070.1:c.1845G>T
|
XP_011535372.1:p.Leu615=
|
|
XM_011537071.1:c.1812G>T
|
XP_011535373.1:p.Leu604=
|
|
XM_011537072.1:c.1791G>T
|
XP_011535374.1:p.Leu597=
|
|
XM_011537073.1:c.1584G>T
|
XP_011535375.1:p.Leu528=
|
|
XM_011537074.1:c.1584G>T
|
XP_011535376.1:p.Leu528=
|
|
XM_005267991.3:c.1998G>T
|
XP_005268048.2:p.Leu666=
|
|
XM_005267992.3:c.1992G>T
|
XP_005268049.2:p.Leu664=
|
|
XM_011537067.2:c.1941G>T
|
XP_011535369.1:p.Leu647=
|
|
XM_011537069.2:c.1989G>T
|
XP_011535371.2:p.Leu663=
|
|
XM_011537070.2:c.1845G>T
|
XP_011535372.1:p.Leu615=
|
|
XM_011537071.2:c.1899G>T
|
XP_011535373.2:p.Leu633=
|
|
XM_011537072.2:c.1791G>T
|
XP_011535374.1:p.Leu597=
|
|
XM_017021582.1:c.2049G>T
|
XP_016877071.1:p.Leu683=
|
|
XM_017021583.1:c.2040G>T
|
XP_016877072.1:p.Leu680=
|
|
XM_017021584.1:c.1959G>T
|
XP_016877073.1:p.Leu653=
|
|
XM_017021585.1:c.1908G>T
|
XP_016877074.1:p.Leu636=
|
|
XM_017021586.1:c.1584G>T
|
XP_016877075.1:p.Leu528=
|
|
XM_017021587.1:c.1584G>T
|
XP_016877076.1:p.Leu528=
|
|
XM_017021588.1:c.1584G>T
|
XP_016877077.1:p.Leu528=
|
|
NM_001164749.2:c.1890G>T
MANE Select
|
NP_001158221.1:p.Leu630=
|
|
NM_001165893.2:c.1800G>T
|
NP_001159365.1:p.Leu600=
|
|
NM_022123.3:c.1794G>T
|
NP_071406.1:p.Leu598=
|
|
NM_173159.3:c.1851G>T
|
NP_775182.1:p.Leu617=
|
|
NM_001394988.1:c.1845G>T
|
NP_001381917.1:p.Leu615=
|
|
NM_001394989.1:c.1791G>T
|
NP_001381918.1:p.Leu597=
|
|