ENST00000704099.1:c.12673C>T
|
ENSP00000515693.1:p.Leu4225Phe
|
|
ENST00000262854.11:c.12889C>T
MANE Select
|
ENSP00000262854.6:p.Leu4297Phe
|
|
ENST00000262854.10:c.12889C>T
|
ENSP00000262854.6:p.Leu4297Phe
|
|
ENST00000342160.7:c.12889C>T
|
ENSP00000340648.3:p.Leu4297Phe
|
|
ENST00000426907.5:c.3356C>T
|
|
|
ENST00000488459.1:n.202C>T
|
|
|
ENST00000612484.4:c.12862C>T
|
ENSP00000479451.1:p.Leu4288Phe
|
|
NM_031407.6:c.12889C>T
|
NP_113584.3:p.Leu4297Phe
|
|
XM_005261965.2:c.12889C>T
|
XP_005262022.1:p.Leu4297Phe
|
|
XM_011530746.1:c.13138C>T
|
XP_011529048.1:p.Leu4380Phe
|
|
XM_011530747.1:c.13138C>T
|
XP_011529049.1:p.Leu4380Phe
|
|
XM_011530748.1:c.13138C>T
|
XP_011529050.1:p.Leu4380Phe
|
|
XM_011530749.1:c.13138C>T
|
XP_011529051.1:p.Leu4380Phe
|
|
XM_011530750.1:c.13138C>T
|
XP_011529052.1:p.Leu4380Phe
|
|
XM_011530751.1:c.13138C>T
|
XP_011529053.1:p.Leu4380Phe
|
|
XM_011530752.1:c.13135C>T
|
XP_011529054.1:p.Leu4379Phe
|
|
XM_011530753.1:c.13093C>T
|
XP_011529055.1:p.Leu4365Phe
|
|
XM_011530754.1:c.13090C>T
|
XP_011529056.1:p.Leu4364Phe
|
|
XM_011530755.1:c.13087C>T
|
XP_011529057.1:p.Leu4363Phe
|
|
XM_011530756.1:c.13039C>T
|
XP_011529058.1:p.Leu4347Phe
|
|
XM_011530757.1:c.12736C>T
|
XP_011529059.1:p.Leu4246Phe
|
|
XM_005261965.4:c.12889C>T
|
XP_005262022.1:p.Leu4297Phe
|
|
XM_011530751.2:c.13138C>T
|
XP_011529053.1:p.Leu4380Phe
|
|
XM_017029191.1:c.13270C>T
|
XP_016884680.1:p.Leu4424Phe
|
|
XM_017029192.1:c.13267C>T
|
XP_016884681.1:p.Leu4423Phe
|
|
XM_017029193.1:c.13249C>T
|
XP_016884682.1:p.Leu4417Phe
|
|
XM_017029194.1:c.13225C>T
|
XP_016884683.1:p.Leu4409Phe
|
|
XM_017029195.1:c.13222C>T
|
XP_016884684.1:p.Leu4408Phe
|
|
XM_017029196.1:c.13219C>T
|
XP_016884685.1:p.Leu4407Phe
|
|
XM_017029197.1:c.13171C>T
|
XP_016884686.1:p.Leu4391Phe
|
|
XM_017029198.2:c.13159C>T
|
XP_016884687.1:p.Leu4387Phe
|
|
XM_017029199.1:c.13159C>T
|
XP_016884688.1:p.Leu4387Phe
|
|
XM_017029200.1:c.13159C>T
|
XP_016884689.1:p.Leu4387Phe
|
|
XM_017029201.1:c.13159C>T
|
XP_016884690.1:p.Leu4387Phe
|
|
XM_017029202.1:c.13159C>T
|
XP_016884691.1:p.Leu4387Phe
|
|
XM_017029203.1:c.13159C>T
|
XP_016884692.1:p.Leu4387Phe
|
|
XM_017029204.1:c.13021C>T
|
XP_016884693.1:p.Leu4341Phe
|
|
XM_017029206.1:c.12868C>T
|
XP_016884695.1:p.Leu4290Phe
|
|
XM_024452322.1:c.13138C>T
|
XP_024308090.1:p.Leu4380Phe
|
|
NM_031407.7:c.12889C>T
MANE Select
|
NP_113584.3:p.Leu4297Phe
|
|