ENST00000356141.9:c.1818G>A
MANE Select
|
ENSP00000348460.4:p.Arg606=
|
|
ENST00000551634.6:c.1827G>A
|
ENSP00000448373.2:p.Arg609=
|
|
ENST00000680362.1:c.1718G>A
|
|
|
ENST00000681323.1:c.793+2544G>A
|
|
|
ENST00000346562.6:c.1722G>A
|
ENSP00000319610.5:p.Arg574=
|
|
ENST00000356141.8:c.1818G>A
|
ENSP00000348460.4:p.Arg606=
|
|
ENST00000357798.9:c.1779G>A
|
ENSP00000350446.5:p.Arg593=
|
|
ENST00000548645.5:c.1728G>A
|
ENSP00000448916.1:p.Arg576=
|
|
ENST00000551492.5:c.1833G>A
|
ENSP00000450392.1:p.Arg611=
|
|
ENST00000551634.5:c.1740G>A
|
ENSP00000448373.1:p.Arg580=
|
|
NM_001164749.1:c.1818G>A
|
NP_001158221.1:p.Arg606=
|
|
NM_001165893.1:c.1728G>A
|
NP_001159365.1:p.Arg576=
|
|
NM_022123.2:c.1722G>A
|
NP_071406.1:p.Arg574=
|
|
NM_173159.2:c.1779G>A
|
NP_775182.1:p.Arg593=
|
|
XM_005267991.2:c.1839G>A
|
XP_005268048.1:p.Arg613=
|
|
XM_005267992.2:c.1833G>A
|
XP_005268049.1:p.Arg611=
|
|
XM_005267993.2:c.1779G>A
|
XP_005268050.1:p.Arg593=
|
|
XM_011537067.1:c.1869G>A
|
XP_011535369.1:p.Arg623=
|
|
XM_011537068.1:c.1860G>A
|
XP_011535370.1:p.Arg620=
|
|
XM_011537069.1:c.1830G>A
|
XP_011535371.1:p.Arg610=
|
|
XM_011537070.1:c.1773G>A
|
XP_011535372.1:p.Arg591=
|
|
XM_011537071.1:c.1740G>A
|
XP_011535373.1:p.Arg580=
|
|
XM_011537072.1:c.1719G>A
|
XP_011535374.1:p.Arg573=
|
|
XM_011537073.1:c.1512G>A
|
XP_011535375.1:p.Arg504=
|
|
XM_011537074.1:c.1512G>A
|
XP_011535376.1:p.Arg504=
|
|
XM_005267991.3:c.1926G>A
|
XP_005268048.2:p.Arg642=
|
|
XM_005267992.3:c.1920G>A
|
XP_005268049.2:p.Arg640=
|
|
XM_011537067.2:c.1869G>A
|
XP_011535369.1:p.Arg623=
|
|
XM_011537069.2:c.1917G>A
|
XP_011535371.2:p.Arg639=
|
|
XM_011537070.2:c.1773G>A
|
XP_011535372.1:p.Arg591=
|
|
XM_011537071.2:c.1827G>A
|
XP_011535373.2:p.Arg609=
|
|
XM_011537072.2:c.1719G>A
|
XP_011535374.1:p.Arg573=
|
|
XM_017021582.1:c.1977G>A
|
XP_016877071.1:p.Arg659=
|
|
XM_017021583.1:c.1968G>A
|
XP_016877072.1:p.Arg656=
|
|
XM_017021584.1:c.1887G>A
|
XP_016877073.1:p.Arg629=
|
|
XM_017021585.1:c.1836G>A
|
XP_016877074.1:p.Arg612=
|
|
XM_017021586.1:c.1512G>A
|
XP_016877075.1:p.Arg504=
|
|
XM_017021587.1:c.1512G>A
|
XP_016877076.1:p.Arg504=
|
|
XM_017021588.1:c.1512G>A
|
XP_016877077.1:p.Arg504=
|
|
NM_001164749.2:c.1818G>A
MANE Select
|
NP_001158221.1:p.Arg606=
|
|
NM_001165893.2:c.1728G>A
|
NP_001159365.1:p.Arg576=
|
|
NM_022123.3:c.1722G>A
|
NP_071406.1:p.Arg574=
|
|
NM_173159.3:c.1779G>A
|
NP_775182.1:p.Arg593=
|
|
NM_001394988.1:c.1773G>A
|
NP_001381917.1:p.Arg591=
|
|
NM_001394989.1:c.1719G>A
|
NP_001381918.1:p.Arg573=
|
|