ENST00000704099.1:c.12668A>C
|
ENSP00000515693.1:p.Lys4223Thr
|
|
ENST00000262854.11:c.12884A>C
MANE Select
|
ENSP00000262854.6:p.Lys4295Thr
|
|
ENST00000262854.10:c.12884A>C
|
ENSP00000262854.6:p.Lys4295Thr
|
|
ENST00000342160.7:c.12884A>C
|
ENSP00000340648.3:p.Lys4295Thr
|
|
ENST00000426907.5:c.3351A>C
|
|
|
ENST00000488459.1:n.197A>C
|
|
|
ENST00000612484.4:c.12857A>C
|
ENSP00000479451.1:p.Lys4286Thr
|
|
NM_031407.6:c.12884A>C
|
NP_113584.3:p.Lys4295Thr
|
|
XM_005261965.2:c.12884A>C
|
XP_005262022.1:p.Lys4295Thr
|
|
XM_011530746.1:c.13133A>C
|
XP_011529048.1:p.Lys4378Thr
|
|
XM_011530747.1:c.13133A>C
|
XP_011529049.1:p.Lys4378Thr
|
|
XM_011530748.1:c.13133A>C
|
XP_011529050.1:p.Lys4378Thr
|
|
XM_011530749.1:c.13133A>C
|
XP_011529051.1:p.Lys4378Thr
|
|
XM_011530750.1:c.13133A>C
|
XP_011529052.1:p.Lys4378Thr
|
|
XM_011530751.1:c.13133A>C
|
XP_011529053.1:p.Lys4378Thr
|
|
XM_011530752.1:c.13130A>C
|
XP_011529054.1:p.Lys4377Thr
|
|
XM_011530753.1:c.13088A>C
|
XP_011529055.1:p.Lys4363Thr
|
|
XM_011530754.1:c.13085A>C
|
XP_011529056.1:p.Lys4362Thr
|
|
XM_011530755.1:c.13082A>C
|
XP_011529057.1:p.Lys4361Thr
|
|
XM_011530756.1:c.13034A>C
|
XP_011529058.1:p.Lys4345Thr
|
|
XM_011530757.1:c.12731A>C
|
XP_011529059.1:p.Lys4244Thr
|
|
XM_005261965.4:c.12884A>C
|
XP_005262022.1:p.Lys4295Thr
|
|
XM_011530751.2:c.13133A>C
|
XP_011529053.1:p.Lys4378Thr
|
|
XM_017029191.1:c.13265A>C
|
XP_016884680.1:p.Lys4422Thr
|
|
XM_017029192.1:c.13262A>C
|
XP_016884681.1:p.Lys4421Thr
|
|
XM_017029193.1:c.13244A>C
|
XP_016884682.1:p.Lys4415Thr
|
|
XM_017029194.1:c.13220A>C
|
XP_016884683.1:p.Lys4407Thr
|
|
XM_017029195.1:c.13217A>C
|
XP_016884684.1:p.Lys4406Thr
|
|
XM_017029196.1:c.13214A>C
|
XP_016884685.1:p.Lys4405Thr
|
|
XM_017029197.1:c.13166A>C
|
XP_016884686.1:p.Lys4389Thr
|
|
XM_017029198.2:c.13154A>C
|
XP_016884687.1:p.Lys4385Thr
|
|
XM_017029199.1:c.13154A>C
|
XP_016884688.1:p.Lys4385Thr
|
|
XM_017029200.1:c.13154A>C
|
XP_016884689.1:p.Lys4385Thr
|
|
XM_017029201.1:c.13154A>C
|
XP_016884690.1:p.Lys4385Thr
|
|
XM_017029202.1:c.13154A>C
|
XP_016884691.1:p.Lys4385Thr
|
|
XM_017029203.1:c.13154A>C
|
XP_016884692.1:p.Lys4385Thr
|
|
XM_017029204.1:c.13016A>C
|
XP_016884693.1:p.Lys4339Thr
|
|
XM_017029206.1:c.12863A>C
|
XP_016884695.1:p.Lys4288Thr
|
|
XM_024452322.1:c.13133A>C
|
XP_024308090.1:p.Lys4378Thr
|
|
NM_031407.7:c.12884A>C
MANE Select
|
NP_113584.3:p.Lys4295Thr
|
|