ENST00000704099.1:c.12605A>C
|
ENSP00000515693.1:p.Asn4202Thr
|
|
ENST00000262854.11:c.12821A>C
MANE Select
|
ENSP00000262854.6:p.Asn4274Thr
|
|
ENST00000262854.10:c.12821A>C
|
ENSP00000262854.6:p.Asn4274Thr
|
|
ENST00000342160.7:c.12821A>C
|
ENSP00000340648.3:p.Asn4274Thr
|
|
ENST00000426907.5:c.3288A>C
|
|
|
ENST00000488459.1:n.134A>C
|
|
|
ENST00000612484.4:c.12794A>C
|
ENSP00000479451.1:p.Asn4265Thr
|
|
NM_031407.6:c.12821A>C
|
NP_113584.3:p.Asn4274Thr
|
|
XM_005261965.2:c.12821A>C
|
XP_005262022.1:p.Asn4274Thr
|
|
XM_011530746.1:c.13070A>C
|
XP_011529048.1:p.Asn4357Thr
|
|
XM_011530747.1:c.13070A>C
|
XP_011529049.1:p.Asn4357Thr
|
|
XM_011530748.1:c.13070A>C
|
XP_011529050.1:p.Asn4357Thr
|
|
XM_011530749.1:c.13070A>C
|
XP_011529051.1:p.Asn4357Thr
|
|
XM_011530750.1:c.13070A>C
|
XP_011529052.1:p.Asn4357Thr
|
|
XM_011530751.1:c.13070A>C
|
XP_011529053.1:p.Asn4357Thr
|
|
XM_011530752.1:c.13067A>C
|
XP_011529054.1:p.Asn4356Thr
|
|
XM_011530753.1:c.13025A>C
|
XP_011529055.1:p.Asn4342Thr
|
|
XM_011530754.1:c.13022A>C
|
XP_011529056.1:p.Asn4341Thr
|
|
XM_011530755.1:c.13019A>C
|
XP_011529057.1:p.Asn4340Thr
|
|
XM_011530756.1:c.12971A>C
|
XP_011529058.1:p.Asn4324Thr
|
|
XM_011530757.1:c.12668A>C
|
XP_011529059.1:p.Asn4223Thr
|
|
XM_005261965.4:c.12821A>C
|
XP_005262022.1:p.Asn4274Thr
|
|
XM_011530751.2:c.13070A>C
|
XP_011529053.1:p.Asn4357Thr
|
|
XM_017029191.1:c.13202A>C
|
XP_016884680.1:p.Asn4401Thr
|
|
XM_017029192.1:c.13199A>C
|
XP_016884681.1:p.Asn4400Thr
|
|
XM_017029193.1:c.13181A>C
|
XP_016884682.1:p.Asn4394Thr
|
|
XM_017029194.1:c.13157A>C
|
XP_016884683.1:p.Asn4386Thr
|
|
XM_017029195.1:c.13154A>C
|
XP_016884684.1:p.Asn4385Thr
|
|
XM_017029196.1:c.13151A>C
|
XP_016884685.1:p.Asn4384Thr
|
|
XM_017029197.1:c.13103A>C
|
XP_016884686.1:p.Asn4368Thr
|
|
XM_017029198.2:c.13091A>C
|
XP_016884687.1:p.Asn4364Thr
|
|
XM_017029199.1:c.13091A>C
|
XP_016884688.1:p.Asn4364Thr
|
|
XM_017029200.1:c.13091A>C
|
XP_016884689.1:p.Asn4364Thr
|
|
XM_017029201.1:c.13091A>C
|
XP_016884690.1:p.Asn4364Thr
|
|
XM_017029202.1:c.13091A>C
|
XP_016884691.1:p.Asn4364Thr
|
|
XM_017029203.1:c.13091A>C
|
XP_016884692.1:p.Asn4364Thr
|
|
XM_017029204.1:c.12953A>C
|
XP_016884693.1:p.Asn4318Thr
|
|
XM_017029206.1:c.12800A>C
|
XP_016884695.1:p.Asn4267Thr
|
|
XM_024452322.1:c.13070A>C
|
XP_024308090.1:p.Asn4357Thr
|
|
NM_031407.7:c.12821A>C
MANE Select
|
NP_113584.3:p.Asn4274Thr
|
|