ENST00000704099.1:c.12650A>G
|
ENSP00000515693.1:p.Asp4217Gly
|
|
ENST00000262854.11:c.12866A>G
MANE Select
|
ENSP00000262854.6:p.Asp4289Gly
|
|
ENST00000262854.10:c.12866A>G
|
ENSP00000262854.6:p.Asp4289Gly
|
|
ENST00000342160.7:c.12866A>G
|
ENSP00000340648.3:p.Asp4289Gly
|
|
ENST00000426907.5:c.3333A>G
|
|
|
ENST00000488459.1:n.179A>G
|
|
|
ENST00000612484.4:c.12839A>G
|
ENSP00000479451.1:p.Asp4280Gly
|
|
NM_031407.6:c.12866A>G
|
NP_113584.3:p.Asp4289Gly
|
|
XM_005261965.2:c.12866A>G
|
XP_005262022.1:p.Asp4289Gly
|
|
XM_011530746.1:c.13115A>G
|
XP_011529048.1:p.Asp4372Gly
|
|
XM_011530747.1:c.13115A>G
|
XP_011529049.1:p.Asp4372Gly
|
|
XM_011530748.1:c.13115A>G
|
XP_011529050.1:p.Asp4372Gly
|
|
XM_011530749.1:c.13115A>G
|
XP_011529051.1:p.Asp4372Gly
|
|
XM_011530750.1:c.13115A>G
|
XP_011529052.1:p.Asp4372Gly
|
|
XM_011530751.1:c.13115A>G
|
XP_011529053.1:p.Asp4372Gly
|
|
XM_011530752.1:c.13112A>G
|
XP_011529054.1:p.Asp4371Gly
|
|
XM_011530753.1:c.13070A>G
|
XP_011529055.1:p.Asp4357Gly
|
|
XM_011530754.1:c.13067A>G
|
XP_011529056.1:p.Asp4356Gly
|
|
XM_011530755.1:c.13064A>G
|
XP_011529057.1:p.Asp4355Gly
|
|
XM_011530756.1:c.13016A>G
|
XP_011529058.1:p.Asp4339Gly
|
|
XM_011530757.1:c.12713A>G
|
XP_011529059.1:p.Asp4238Gly
|
|
XM_005261965.4:c.12866A>G
|
XP_005262022.1:p.Asp4289Gly
|
|
XM_011530751.2:c.13115A>G
|
XP_011529053.1:p.Asp4372Gly
|
|
XM_017029191.1:c.13247A>G
|
XP_016884680.1:p.Asp4416Gly
|
|
XM_017029192.1:c.13244A>G
|
XP_016884681.1:p.Asp4415Gly
|
|
XM_017029193.1:c.13226A>G
|
XP_016884682.1:p.Asp4409Gly
|
|
XM_017029194.1:c.13202A>G
|
XP_016884683.1:p.Asp4401Gly
|
|
XM_017029195.1:c.13199A>G
|
XP_016884684.1:p.Asp4400Gly
|
|
XM_017029196.1:c.13196A>G
|
XP_016884685.1:p.Asp4399Gly
|
|
XM_017029197.1:c.13148A>G
|
XP_016884686.1:p.Asp4383Gly
|
|
XM_017029198.2:c.13136A>G
|
XP_016884687.1:p.Asp4379Gly
|
|
XM_017029199.1:c.13136A>G
|
XP_016884688.1:p.Asp4379Gly
|
|
XM_017029200.1:c.13136A>G
|
XP_016884689.1:p.Asp4379Gly
|
|
XM_017029201.1:c.13136A>G
|
XP_016884690.1:p.Asp4379Gly
|
|
XM_017029202.1:c.13136A>G
|
XP_016884691.1:p.Asp4379Gly
|
|
XM_017029203.1:c.13136A>G
|
XP_016884692.1:p.Asp4379Gly
|
|
XM_017029204.1:c.12998A>G
|
XP_016884693.1:p.Asp4333Gly
|
|
XM_017029206.1:c.12845A>G
|
XP_016884695.1:p.Asp4282Gly
|
|
XM_024452322.1:c.13115A>G
|
XP_024308090.1:p.Asp4372Gly
|
|
NM_031407.7:c.12866A>G
MANE Select
|
NP_113584.3:p.Asp4289Gly
|
|