|
ENST00000276072.9:c.3983G>A
|
ENSP00000276072.5:p.Arg1328Gln
|
|
|
ENST00000437147.8:c.658G>A
|
|
|
|
ENST00000461764.6:c.683G>A
|
|
|
|
ENST00000468167.6:n.175G>A
|
|
|
|
ENST00000485087.6:c.658G>A
|
|
|
|
ENST00000492404.6:n.1308G>A
|
|
|
|
ENST00000682124.1:c.615G>A
|
|
|
|
ENST00000683202.1:c.4697G>A
|
ENSP00000507781.1:p.Arg1566Gln
|
|
|
ENST00000683358.1:c.658G>A
|
|
|
|
ENST00000683668.1:c.3983G>A
|
ENSP00000507280.1:p.Arg1328Gln
|
|
|
ENST00000683782.1:c.4697G>A
|
ENSP00000506996.1:p.Arg1566Gln
|
|
|
ENST00000683954.1:c.62G>A
|
ENSP00000507714.1:p.Arg21Gln
|
|
|
ENST00000276072.8:c.1291G>A
|
|
|
|
ENST00000373790.9:c.4634G>A
|
ENSP00000362895.5:p.Arg1545Gln
|
|
|
ENST00000423759.6:c.4697G>A
MANE Select
|
ENSP00000406549.2:p.Arg1566Gln
|
|
|
ENST00000276072.7:c.4757G>A
|
ENSP00000276072.3:p.Arg1586Gln
|
|
|
ENST00000373775.8:c.658G>A
|
|
|
|
ENST00000373790.8:c.4694G>A
|
ENSP00000362895.4:p.Arg1565Gln
|
|
|
ENST00000423759.5:c.4757G>A
|
ENSP00000406549.1:p.Arg1586Gln
|
|
|
ENST00000437147.7:c.658G>A
|
|
|
|
ENST00000461764.5:n.204G>A
|
|
|
|
ENST00000462588.5:n.204G>A
|
|
|
|
ENST00000468167.5:n.204G>A
|
|
|
|
ENST00000485087.5:n.204G>A
|
|
|
|
ENST00000492404.5:n.118G>A
|
|
|
|
NM_001286074.1:c.4757G>A
|
NP_001273003.1:p.Arg1586Gln
|
|
|
NM_004606.4:c.4757G>A
|
NP_004597.2:p.Arg1586Gln
|
|
|
NM_138923.3:c.4694G>A
|
NP_620278.1:p.Arg1565Gln
|
|
|
NR_104387.1:n.4833G>A
|
|
|
|
NR_104388.1:n.4833G>A
|
|
|
|
NR_104389.1:n.4833G>A
|
|
|
|
NR_104390.1:n.4833G>A
|
|
|
|
NR_104391.1:n.4833G>A
|
|
|
|
NR_104392.1:n.4833G>A
|
|
|
|
NR_104393.1:n.4833G>A
|
|
|
|
NR_104394.1:n.4790G>A
|
|
|
|
NR_104395.1:n.4858G>A
|
|
|
|
XM_005262295.1:c.4757G>A
|
XP_005262352.1:p.Arg1586Gln
|
|
|
XM_005262296.1:c.4754G>A
|
XP_005262353.1:p.Arg1585Gln
|
|
|
XM_005262297.3:c.4694G>A
|
XP_005262354.1:p.Arg1565Gln
|
|
|
XM_006724682.2:c.4376G>A
|
XP_006724745.1:p.Arg1459Gln
|
|
|
XM_011531016.1:c.4757G>A
|
XP_011529318.1:p.Arg1586Gln
|
|
|
XM_005262297.4:c.4694G>A
|
XP_005262354.1:p.Arg1565Gln
|
|
|
XM_024452429.1:c.4376G>A
|
XP_024308197.1:p.Arg1459Gln
|
|
|
XM_024452430.1:c.4757G>A
|
XP_024308198.1:p.Arg1586Gln
|
|
|
NM_001286074.2:c.4697G>A
|
NP_001273003.2:p.Arg1566Gln
|
|
|
NM_004606.5:c.4697G>A
MANE Select
|
NP_004597.3:p.Arg1566Gln
|
|
|
NM_138923.4:c.4634G>A
|
NP_620278.2:p.Arg1545Gln
|
|
|
NR_104387.2:n.4715G>A
|
|
|
|
NR_104388.2:n.4715G>A
|
|
|
|
NR_104389.2:n.4715G>A
|
|
|
|
NR_104390.2:n.4715G>A
|
|
|
|
NR_104391.2:n.4715G>A
|
|
|
|
NR_104392.2:n.4715G>A
|
|
|
|
NR_104393.2:n.4715G>A
|
|
|
|
NR_104394.2:n.4672G>A
|
|
|
|
NR_104395.2:n.4740G>A
|
|
|
