ENST00000276072.9:c.2951G>T
|
ENSP00000276072.5:p.Arg984Leu
|
|
ENST00000483985.3:c.580G>T
|
|
|
ENST00000683202.1:c.3665G>T
|
ENSP00000507781.1:p.Arg1222Leu
|
|
ENST00000683668.1:c.2951G>T
|
ENSP00000507280.1:p.Arg984Leu
|
|
ENST00000683782.1:c.3665G>T
|
ENSP00000506996.1:p.Arg1222Leu
|
|
ENST00000276072.8:c.259G>T
|
|
|
ENST00000373790.9:c.3602G>T
|
ENSP00000362895.5:p.Arg1201Leu
|
|
ENST00000423759.6:c.3665G>T
MANE Select
|
ENSP00000406549.2:p.Arg1222Leu
|
|
ENST00000276072.7:c.3725G>T
|
ENSP00000276072.3:p.Arg1242Leu
|
|
ENST00000373790.8:c.3662G>T
|
ENSP00000362895.4:p.Arg1221Leu
|
|
ENST00000423759.5:c.3725G>T
|
ENSP00000406549.1:p.Arg1242Leu
|
|
ENST00000483985.2:c.394G>T
|
|
|
NM_001286074.1:c.3725G>T
|
NP_001273003.1:p.Arg1242Leu
|
|
NM_004606.4:c.3725G>T
|
NP_004597.2:p.Arg1242Leu
|
|
NM_138923.3:c.3662G>T
|
NP_620278.1:p.Arg1221Leu
|
|
NR_104387.1:n.3801G>T
|
|
|
NR_104388.1:n.3801G>T
|
|
|
NR_104389.1:n.3801G>T
|
|
|
NR_104390.1:n.3801G>T
|
|
|
NR_104391.1:n.3801G>T
|
|
|
NR_104392.1:n.3801G>T
|
|
|
NR_104393.1:n.3801G>T
|
|
|
NR_104394.1:n.3801G>T
|
|
|
NR_104395.1:n.3801G>T
|
|
|
XM_005262295.1:c.3725G>T
|
XP_005262352.1:p.Arg1242Leu
|
|
XM_005262296.1:c.3722G>T
|
XP_005262353.1:p.Arg1241Leu
|
|
XM_005262297.3:c.3662G>T
|
XP_005262354.1:p.Arg1221Leu
|
|
XM_006724682.2:c.3344G>T
|
XP_006724745.1:p.Arg1115Leu
|
|
XM_011531016.1:c.3725G>T
|
XP_011529318.1:p.Arg1242Leu
|
|
XR_938407.1:n.3735G>T
|
|
|
XM_005262297.4:c.3662G>T
|
XP_005262354.1:p.Arg1221Leu
|
|
XM_024452429.1:c.3344G>T
|
XP_024308197.1:p.Arg1115Leu
|
|
XM_024452430.1:c.3725G>T
|
XP_024308198.1:p.Arg1242Leu
|
|
NM_001286074.2:c.3665G>T
|
NP_001273003.2:p.Arg1222Leu
|
|
NM_004606.5:c.3665G>T
MANE Select
|
NP_004597.3:p.Arg1222Leu
|
|
NM_138923.4:c.3602G>T
|
NP_620278.2:p.Arg1201Leu
|
|
NR_104387.2:n.3683G>T
|
|
|
NR_104388.2:n.3683G>T
|
|
|
NR_104389.2:n.3683G>T
|
|
|
NR_104390.2:n.3683G>T
|
|
|
NR_104391.2:n.3683G>T
|
|
|
NR_104392.2:n.3683G>T
|
|
|
NR_104393.2:n.3683G>T
|
|
|
NR_104394.2:n.3683G>T
|
|
|
NR_104395.2:n.3683G>T
|
|
|