ENST00000704099.1:c.12625T>C
|
ENSP00000515693.1:p.Phe4209Leu
|
|
ENST00000262854.11:c.12841T>C
MANE Select
|
ENSP00000262854.6:p.Phe4281Leu
|
|
ENST00000262854.10:c.12841T>C
|
ENSP00000262854.6:p.Phe4281Leu
|
|
ENST00000342160.7:c.12841T>C
|
ENSP00000340648.3:p.Phe4281Leu
|
|
ENST00000426907.5:c.3308T>C
|
|
|
ENST00000488459.1:n.154T>C
|
|
|
ENST00000612484.4:c.12814T>C
|
ENSP00000479451.1:p.Phe4272Leu
|
|
NM_031407.6:c.12841T>C
|
NP_113584.3:p.Phe4281Leu
|
|
XM_005261965.2:c.12841T>C
|
XP_005262022.1:p.Phe4281Leu
|
|
XM_011530746.1:c.13090T>C
|
XP_011529048.1:p.Phe4364Leu
|
|
XM_011530747.1:c.13090T>C
|
XP_011529049.1:p.Phe4364Leu
|
|
XM_011530748.1:c.13090T>C
|
XP_011529050.1:p.Phe4364Leu
|
|
XM_011530749.1:c.13090T>C
|
XP_011529051.1:p.Phe4364Leu
|
|
XM_011530750.1:c.13090T>C
|
XP_011529052.1:p.Phe4364Leu
|
|
XM_011530751.1:c.13090T>C
|
XP_011529053.1:p.Phe4364Leu
|
|
XM_011530752.1:c.13087T>C
|
XP_011529054.1:p.Phe4363Leu
|
|
XM_011530753.1:c.13045T>C
|
XP_011529055.1:p.Phe4349Leu
|
|
XM_011530754.1:c.13042T>C
|
XP_011529056.1:p.Phe4348Leu
|
|
XM_011530755.1:c.13039T>C
|
XP_011529057.1:p.Phe4347Leu
|
|
XM_011530756.1:c.12991T>C
|
XP_011529058.1:p.Phe4331Leu
|
|
XM_011530757.1:c.12688T>C
|
XP_011529059.1:p.Phe4230Leu
|
|
XM_005261965.4:c.12841T>C
|
XP_005262022.1:p.Phe4281Leu
|
|
XM_011530751.2:c.13090T>C
|
XP_011529053.1:p.Phe4364Leu
|
|
XM_017029191.1:c.13222T>C
|
XP_016884680.1:p.Phe4408Leu
|
|
XM_017029192.1:c.13219T>C
|
XP_016884681.1:p.Phe4407Leu
|
|
XM_017029193.1:c.13201T>C
|
XP_016884682.1:p.Phe4401Leu
|
|
XM_017029194.1:c.13177T>C
|
XP_016884683.1:p.Phe4393Leu
|
|
XM_017029195.1:c.13174T>C
|
XP_016884684.1:p.Phe4392Leu
|
|
XM_017029196.1:c.13171T>C
|
XP_016884685.1:p.Phe4391Leu
|
|
XM_017029197.1:c.13123T>C
|
XP_016884686.1:p.Phe4375Leu
|
|
XM_017029198.2:c.13111T>C
|
XP_016884687.1:p.Phe4371Leu
|
|
XM_017029199.1:c.13111T>C
|
XP_016884688.1:p.Phe4371Leu
|
|
XM_017029200.1:c.13111T>C
|
XP_016884689.1:p.Phe4371Leu
|
|
XM_017029201.1:c.13111T>C
|
XP_016884690.1:p.Phe4371Leu
|
|
XM_017029202.1:c.13111T>C
|
XP_016884691.1:p.Phe4371Leu
|
|
XM_017029203.1:c.13111T>C
|
XP_016884692.1:p.Phe4371Leu
|
|
XM_017029204.1:c.12973T>C
|
XP_016884693.1:p.Phe4325Leu
|
|
XM_017029206.1:c.12820T>C
|
XP_016884695.1:p.Phe4274Leu
|
|
XM_024452322.1:c.13090T>C
|
XP_024308090.1:p.Phe4364Leu
|
|
NM_031407.7:c.12841T>C
MANE Select
|
NP_113584.3:p.Phe4281Leu
|
|