ENST00000704099.1:c.12614A>T
|
ENSP00000515693.1:p.Gln4205Leu
|
|
ENST00000262854.11:c.12830A>T
MANE Select
|
ENSP00000262854.6:p.Gln4277Leu
|
|
ENST00000262854.10:c.12830A>T
|
ENSP00000262854.6:p.Gln4277Leu
|
|
ENST00000342160.7:c.12830A>T
|
ENSP00000340648.3:p.Gln4277Leu
|
|
ENST00000426907.5:c.3297A>T
|
|
|
ENST00000488459.1:n.143A>T
|
|
|
ENST00000612484.4:c.12803A>T
|
ENSP00000479451.1:p.Gln4268Leu
|
|
NM_031407.6:c.12830A>T
|
NP_113584.3:p.Gln4277Leu
|
|
XM_005261965.2:c.12830A>T
|
XP_005262022.1:p.Gln4277Leu
|
|
XM_011530746.1:c.13079A>T
|
XP_011529048.1:p.Gln4360Leu
|
|
XM_011530747.1:c.13079A>T
|
XP_011529049.1:p.Gln4360Leu
|
|
XM_011530748.1:c.13079A>T
|
XP_011529050.1:p.Gln4360Leu
|
|
XM_011530749.1:c.13079A>T
|
XP_011529051.1:p.Gln4360Leu
|
|
XM_011530750.1:c.13079A>T
|
XP_011529052.1:p.Gln4360Leu
|
|
XM_011530751.1:c.13079A>T
|
XP_011529053.1:p.Gln4360Leu
|
|
XM_011530752.1:c.13076A>T
|
XP_011529054.1:p.Gln4359Leu
|
|
XM_011530753.1:c.13034A>T
|
XP_011529055.1:p.Gln4345Leu
|
|
XM_011530754.1:c.13031A>T
|
XP_011529056.1:p.Gln4344Leu
|
|
XM_011530755.1:c.13028A>T
|
XP_011529057.1:p.Gln4343Leu
|
|
XM_011530756.1:c.12980A>T
|
XP_011529058.1:p.Gln4327Leu
|
|
XM_011530757.1:c.12677A>T
|
XP_011529059.1:p.Gln4226Leu
|
|
XM_005261965.4:c.12830A>T
|
XP_005262022.1:p.Gln4277Leu
|
|
XM_011530751.2:c.13079A>T
|
XP_011529053.1:p.Gln4360Leu
|
|
XM_017029191.1:c.13211A>T
|
XP_016884680.1:p.Gln4404Leu
|
|
XM_017029192.1:c.13208A>T
|
XP_016884681.1:p.Gln4403Leu
|
|
XM_017029193.1:c.13190A>T
|
XP_016884682.1:p.Gln4397Leu
|
|
XM_017029194.1:c.13166A>T
|
XP_016884683.1:p.Gln4389Leu
|
|
XM_017029195.1:c.13163A>T
|
XP_016884684.1:p.Gln4388Leu
|
|
XM_017029196.1:c.13160A>T
|
XP_016884685.1:p.Gln4387Leu
|
|
XM_017029197.1:c.13112A>T
|
XP_016884686.1:p.Gln4371Leu
|
|
XM_017029198.2:c.13100A>T
|
XP_016884687.1:p.Gln4367Leu
|
|
XM_017029199.1:c.13100A>T
|
XP_016884688.1:p.Gln4367Leu
|
|
XM_017029200.1:c.13100A>T
|
XP_016884689.1:p.Gln4367Leu
|
|
XM_017029201.1:c.13100A>T
|
XP_016884690.1:p.Gln4367Leu
|
|
XM_017029202.1:c.13100A>T
|
XP_016884691.1:p.Gln4367Leu
|
|
XM_017029203.1:c.13100A>T
|
XP_016884692.1:p.Gln4367Leu
|
|
XM_017029204.1:c.12962A>T
|
XP_016884693.1:p.Gln4321Leu
|
|
XM_017029206.1:c.12809A>T
|
XP_016884695.1:p.Gln4270Leu
|
|
XM_024452322.1:c.13079A>T
|
XP_024308090.1:p.Gln4360Leu
|
|
NM_031407.7:c.12830A>T
MANE Select
|
NP_113584.3:p.Gln4277Leu
|
|