ENST00000704099.1:c.12661C>T
|
ENSP00000515693.1:p.Arg4221Cys
|
|
ENST00000262854.11:c.12877C>T
MANE Select
|
ENSP00000262854.6:p.Arg4293Cys
|
|
ENST00000262854.10:c.12877C>T
|
ENSP00000262854.6:p.Arg4293Cys
|
|
ENST00000342160.7:c.12877C>T
|
ENSP00000340648.3:p.Arg4293Cys
|
|
ENST00000426907.5:c.3344C>T
|
|
|
ENST00000488459.1:n.190C>T
|
|
|
ENST00000612484.4:c.12850C>T
|
ENSP00000479451.1:p.Arg4284Cys
|
|
NM_031407.6:c.12877C>T
|
NP_113584.3:p.Arg4293Cys
|
|
XM_005261965.2:c.12877C>T
|
XP_005262022.1:p.Arg4293Cys
|
|
XM_011530746.1:c.13126C>T
|
XP_011529048.1:p.Arg4376Cys
|
|
XM_011530747.1:c.13126C>T
|
XP_011529049.1:p.Arg4376Cys
|
|
XM_011530748.1:c.13126C>T
|
XP_011529050.1:p.Arg4376Cys
|
|
XM_011530749.1:c.13126C>T
|
XP_011529051.1:p.Arg4376Cys
|
|
XM_011530750.1:c.13126C>T
|
XP_011529052.1:p.Arg4376Cys
|
|
XM_011530751.1:c.13126C>T
|
XP_011529053.1:p.Arg4376Cys
|
|
XM_011530752.1:c.13123C>T
|
XP_011529054.1:p.Arg4375Cys
|
|
XM_011530753.1:c.13081C>T
|
XP_011529055.1:p.Arg4361Cys
|
|
XM_011530754.1:c.13078C>T
|
XP_011529056.1:p.Arg4360Cys
|
|
XM_011530755.1:c.13075C>T
|
XP_011529057.1:p.Arg4359Cys
|
|
XM_011530756.1:c.13027C>T
|
XP_011529058.1:p.Arg4343Cys
|
|
XM_011530757.1:c.12724C>T
|
XP_011529059.1:p.Arg4242Cys
|
|
XM_005261965.4:c.12877C>T
|
XP_005262022.1:p.Arg4293Cys
|
|
XM_011530751.2:c.13126C>T
|
XP_011529053.1:p.Arg4376Cys
|
|
XM_017029191.1:c.13258C>T
|
XP_016884680.1:p.Arg4420Cys
|
|
XM_017029192.1:c.13255C>T
|
XP_016884681.1:p.Arg4419Cys
|
|
XM_017029193.1:c.13237C>T
|
XP_016884682.1:p.Arg4413Cys
|
|
XM_017029194.1:c.13213C>T
|
XP_016884683.1:p.Arg4405Cys
|
|
XM_017029195.1:c.13210C>T
|
XP_016884684.1:p.Arg4404Cys
|
|
XM_017029196.1:c.13207C>T
|
XP_016884685.1:p.Arg4403Cys
|
|
XM_017029197.1:c.13159C>T
|
XP_016884686.1:p.Arg4387Cys
|
|
XM_017029198.2:c.13147C>T
|
XP_016884687.1:p.Arg4383Cys
|
|
XM_017029199.1:c.13147C>T
|
XP_016884688.1:p.Arg4383Cys
|
|
XM_017029200.1:c.13147C>T
|
XP_016884689.1:p.Arg4383Cys
|
|
XM_017029201.1:c.13147C>T
|
XP_016884690.1:p.Arg4383Cys
|
|
XM_017029202.1:c.13147C>T
|
XP_016884691.1:p.Arg4383Cys
|
|
XM_017029203.1:c.13147C>T
|
XP_016884692.1:p.Arg4383Cys
|
|
XM_017029204.1:c.13009C>T
|
XP_016884693.1:p.Arg4337Cys
|
|
XM_017029206.1:c.12856C>T
|
XP_016884695.1:p.Arg4286Cys
|
|
XM_024452322.1:c.13126C>T
|
XP_024308090.1:p.Arg4376Cys
|
|
NM_031407.7:c.12877C>T
MANE Select
|
NP_113584.3:p.Arg4293Cys
|
|