ENST00000704099.1:c.11911A>T
|
ENSP00000515693.1:p.Lys3971Ter
|
|
ENST00000262854.11:c.12127A>T
MANE Select
|
ENSP00000262854.6:p.Lys4043Ter
|
|
ENST00000262854.10:c.12127A>T
|
ENSP00000262854.6:p.Lys4043Ter
|
|
ENST00000342160.7:c.12127A>T
|
ENSP00000340648.3:p.Lys4043Ter
|
|
ENST00000426907.5:c.2594A>T
|
|
|
ENST00000480438.1:n.262A>T
|
|
|
ENST00000612484.4:c.12100A>T
|
ENSP00000479451.1:p.Lys4034Ter
|
|
NM_031407.6:c.12127A>T
|
NP_113584.3:p.Lys4043Ter
|
|
XM_005261965.2:c.12127A>T
|
XP_005262022.1:p.Lys4043Ter
|
|
XM_011530746.1:c.12376A>T
|
XP_011529048.1:p.Lys4126Ter
|
|
XM_011530747.1:c.12376A>T
|
XP_011529049.1:p.Lys4126Ter
|
|
XM_011530748.1:c.12376A>T
|
XP_011529050.1:p.Lys4126Ter
|
|
XM_011530749.1:c.12376A>T
|
XP_011529051.1:p.Lys4126Ter
|
|
XM_011530750.1:c.12376A>T
|
XP_011529052.1:p.Lys4126Ter
|
|
XM_011530751.1:c.12376A>T
|
XP_011529053.1:p.Lys4126Ter
|
|
XM_011530752.1:c.12373A>T
|
XP_011529054.1:p.Lys4125Ter
|
|
XM_011530753.1:c.12331A>T
|
XP_011529055.1:p.Lys4111Ter
|
|
XM_011530754.1:c.12328A>T
|
XP_011529056.1:p.Lys4110Ter
|
|
XM_011530755.1:c.12325A>T
|
XP_011529057.1:p.Lys4109Ter
|
|
XM_011530756.1:c.12277A>T
|
XP_011529058.1:p.Lys4093Ter
|
|
XM_011530757.1:c.11974A>T
|
XP_011529059.1:p.Lys3992Ter
|
|
XM_005261965.4:c.12127A>T
|
XP_005262022.1:p.Lys4043Ter
|
|
XM_011530751.2:c.12376A>T
|
XP_011529053.1:p.Lys4126Ter
|
|
XM_017029191.1:c.12508A>T
|
XP_016884680.1:p.Lys4170Ter
|
|
XM_017029192.1:c.12505A>T
|
XP_016884681.1:p.Lys4169Ter
|
|
XM_017029193.1:c.12487A>T
|
XP_016884682.1:p.Lys4163Ter
|
|
XM_017029194.1:c.12463A>T
|
XP_016884683.1:p.Lys4155Ter
|
|
XM_017029195.1:c.12460A>T
|
XP_016884684.1:p.Lys4154Ter
|
|
XM_017029196.1:c.12457A>T
|
XP_016884685.1:p.Lys4153Ter
|
|
XM_017029197.1:c.12409A>T
|
XP_016884686.1:p.Lys4137Ter
|
|
XM_017029198.2:c.12397A>T
|
XP_016884687.1:p.Lys4133Ter
|
|
XM_017029199.1:c.12397A>T
|
XP_016884688.1:p.Lys4133Ter
|
|
XM_017029200.1:c.12397A>T
|
XP_016884689.1:p.Lys4133Ter
|
|
XM_017029201.1:c.12397A>T
|
XP_016884690.1:p.Lys4133Ter
|
|
XM_017029202.1:c.12397A>T
|
XP_016884691.1:p.Lys4133Ter
|
|
XM_017029203.1:c.12397A>T
|
XP_016884692.1:p.Lys4133Ter
|
|
XM_017029204.1:c.12259A>T
|
XP_016884693.1:p.Lys4087Ter
|
|
XM_017029206.1:c.12106A>T
|
XP_016884695.1:p.Lys4036Ter
|
|
XM_024452322.1:c.12376A>T
|
XP_024308090.1:p.Lys4126Ter
|
|
NM_031407.7:c.12127A>T
MANE Select
|
NP_113584.3:p.Lys4043Ter
|
|