ENST00000704099.1:c.11821C>T
|
ENSP00000515693.1:p.Arg3941Trp
|
|
ENST00000262854.11:c.12037C>T
MANE Select
|
ENSP00000262854.6:p.Arg4013Trp
|
|
ENST00000262854.10:c.12037C>T
|
ENSP00000262854.6:p.Arg4013Trp
|
|
ENST00000342160.7:c.12037C>T
|
ENSP00000340648.3:p.Arg4013Trp
|
|
ENST00000426907.5:c.2504C>T
|
|
|
ENST00000480438.1:n.172C>T
|
|
|
ENST00000612484.4:c.12010C>T
|
ENSP00000479451.1:p.Arg4004Trp
|
|
NM_031407.6:c.12037C>T
|
NP_113584.3:p.Arg4013Trp
|
|
XM_005261965.2:c.12037C>T
|
XP_005262022.1:p.Arg4013Trp
|
|
XM_011530746.1:c.12286C>T
|
XP_011529048.1:p.Arg4096Trp
|
|
XM_011530747.1:c.12286C>T
|
XP_011529049.1:p.Arg4096Trp
|
|
XM_011530748.1:c.12286C>T
|
XP_011529050.1:p.Arg4096Trp
|
|
XM_011530749.1:c.12286C>T
|
XP_011529051.1:p.Arg4096Trp
|
|
XM_011530750.1:c.12286C>T
|
XP_011529052.1:p.Arg4096Trp
|
|
XM_011530751.1:c.12286C>T
|
XP_011529053.1:p.Arg4096Trp
|
|
XM_011530752.1:c.12283C>T
|
XP_011529054.1:p.Arg4095Trp
|
|
XM_011530753.1:c.12241C>T
|
XP_011529055.1:p.Arg4081Trp
|
|
XM_011530754.1:c.12238C>T
|
XP_011529056.1:p.Arg4080Trp
|
|
XM_011530755.1:c.12235C>T
|
XP_011529057.1:p.Arg4079Trp
|
|
XM_011530756.1:c.12187C>T
|
XP_011529058.1:p.Arg4063Trp
|
|
XM_011530757.1:c.11884C>T
|
XP_011529059.1:p.Arg3962Trp
|
|
XM_005261965.4:c.12037C>T
|
XP_005262022.1:p.Arg4013Trp
|
|
XM_011530751.2:c.12286C>T
|
XP_011529053.1:p.Arg4096Trp
|
|
XM_017029191.1:c.12418C>T
|
XP_016884680.1:p.Arg4140Trp
|
|
XM_017029192.1:c.12415C>T
|
XP_016884681.1:p.Arg4139Trp
|
|
XM_017029193.1:c.12397C>T
|
XP_016884682.1:p.Arg4133Trp
|
|
XM_017029194.1:c.12373C>T
|
XP_016884683.1:p.Arg4125Trp
|
|
XM_017029195.1:c.12370C>T
|
XP_016884684.1:p.Arg4124Trp
|
|
XM_017029196.1:c.12367C>T
|
XP_016884685.1:p.Arg4123Trp
|
|
XM_017029197.1:c.12319C>T
|
XP_016884686.1:p.Arg4107Trp
|
|
XM_017029198.2:c.12307C>T
|
XP_016884687.1:p.Arg4103Trp
|
|
XM_017029199.1:c.12307C>T
|
XP_016884688.1:p.Arg4103Trp
|
|
XM_017029200.1:c.12307C>T
|
XP_016884689.1:p.Arg4103Trp
|
|
XM_017029201.1:c.12307C>T
|
XP_016884690.1:p.Arg4103Trp
|
|
XM_017029202.1:c.12307C>T
|
XP_016884691.1:p.Arg4103Trp
|
|
XM_017029203.1:c.12307C>T
|
XP_016884692.1:p.Arg4103Trp
|
|
XM_017029204.1:c.12169C>T
|
XP_016884693.1:p.Arg4057Trp
|
|
XM_017029206.1:c.12016C>T
|
XP_016884695.1:p.Arg4006Trp
|
|
XM_024452322.1:c.12286C>T
|
XP_024308090.1:p.Arg4096Trp
|
|
NM_031407.7:c.12037C>T
MANE Select
|
NP_113584.3:p.Arg4013Trp
|
|