ENST00000704099.1:c.12605A>G
|
ENSP00000515693.1:p.Asn4202Ser
|
|
ENST00000262854.11:c.12821A>G
MANE Select
|
ENSP00000262854.6:p.Asn4274Ser
|
|
ENST00000262854.10:c.12821A>G
|
ENSP00000262854.6:p.Asn4274Ser
|
|
ENST00000342160.7:c.12821A>G
|
ENSP00000340648.3:p.Asn4274Ser
|
|
ENST00000426907.5:c.3288A>G
|
|
|
ENST00000488459.1:n.134A>G
|
|
|
ENST00000612484.4:c.12794A>G
|
ENSP00000479451.1:p.Asn4265Ser
|
|
NM_031407.6:c.12821A>G
|
NP_113584.3:p.Asn4274Ser
|
|
XM_005261965.2:c.12821A>G
|
XP_005262022.1:p.Asn4274Ser
|
|
XM_011530746.1:c.13070A>G
|
XP_011529048.1:p.Asn4357Ser
|
|
XM_011530747.1:c.13070A>G
|
XP_011529049.1:p.Asn4357Ser
|
|
XM_011530748.1:c.13070A>G
|
XP_011529050.1:p.Asn4357Ser
|
|
XM_011530749.1:c.13070A>G
|
XP_011529051.1:p.Asn4357Ser
|
|
XM_011530750.1:c.13070A>G
|
XP_011529052.1:p.Asn4357Ser
|
|
XM_011530751.1:c.13070A>G
|
XP_011529053.1:p.Asn4357Ser
|
|
XM_011530752.1:c.13067A>G
|
XP_011529054.1:p.Asn4356Ser
|
|
XM_011530753.1:c.13025A>G
|
XP_011529055.1:p.Asn4342Ser
|
|
XM_011530754.1:c.13022A>G
|
XP_011529056.1:p.Asn4341Ser
|
|
XM_011530755.1:c.13019A>G
|
XP_011529057.1:p.Asn4340Ser
|
|
XM_011530756.1:c.12971A>G
|
XP_011529058.1:p.Asn4324Ser
|
|
XM_011530757.1:c.12668A>G
|
XP_011529059.1:p.Asn4223Ser
|
|
XM_005261965.4:c.12821A>G
|
XP_005262022.1:p.Asn4274Ser
|
|
XM_011530751.2:c.13070A>G
|
XP_011529053.1:p.Asn4357Ser
|
|
XM_017029191.1:c.13202A>G
|
XP_016884680.1:p.Asn4401Ser
|
|
XM_017029192.1:c.13199A>G
|
XP_016884681.1:p.Asn4400Ser
|
|
XM_017029193.1:c.13181A>G
|
XP_016884682.1:p.Asn4394Ser
|
|
XM_017029194.1:c.13157A>G
|
XP_016884683.1:p.Asn4386Ser
|
|
XM_017029195.1:c.13154A>G
|
XP_016884684.1:p.Asn4385Ser
|
|
XM_017029196.1:c.13151A>G
|
XP_016884685.1:p.Asn4384Ser
|
|
XM_017029197.1:c.13103A>G
|
XP_016884686.1:p.Asn4368Ser
|
|
XM_017029198.2:c.13091A>G
|
XP_016884687.1:p.Asn4364Ser
|
|
XM_017029199.1:c.13091A>G
|
XP_016884688.1:p.Asn4364Ser
|
|
XM_017029200.1:c.13091A>G
|
XP_016884689.1:p.Asn4364Ser
|
|
XM_017029201.1:c.13091A>G
|
XP_016884690.1:p.Asn4364Ser
|
|
XM_017029202.1:c.13091A>G
|
XP_016884691.1:p.Asn4364Ser
|
|
XM_017029203.1:c.13091A>G
|
XP_016884692.1:p.Asn4364Ser
|
|
XM_017029204.1:c.12953A>G
|
XP_016884693.1:p.Asn4318Ser
|
|
XM_017029206.1:c.12800A>G
|
XP_016884695.1:p.Asn4267Ser
|
|
XM_024452322.1:c.13070A>G
|
XP_024308090.1:p.Asn4357Ser
|
|
NM_031407.7:c.12821A>G
MANE Select
|
NP_113584.3:p.Asn4274Ser
|
|