ENST00000704099.1:c.11885T>A
|
ENSP00000515693.1:p.Leu3962Gln
|
|
ENST00000262854.11:c.12101T>A
MANE Select
|
ENSP00000262854.6:p.Leu4034Gln
|
|
ENST00000262854.10:c.12101T>A
|
ENSP00000262854.6:p.Leu4034Gln
|
|
ENST00000342160.7:c.12101T>A
|
ENSP00000340648.3:p.Leu4034Gln
|
|
ENST00000426907.5:c.2568T>A
|
|
|
ENST00000480438.1:n.236T>A
|
|
|
ENST00000612484.4:c.12074T>A
|
ENSP00000479451.1:p.Leu4025Gln
|
|
NM_031407.6:c.12101T>A
|
NP_113584.3:p.Leu4034Gln
|
|
XM_005261965.2:c.12101T>A
|
XP_005262022.1:p.Leu4034Gln
|
|
XM_011530746.1:c.12350T>A
|
XP_011529048.1:p.Leu4117Gln
|
|
XM_011530747.1:c.12350T>A
|
XP_011529049.1:p.Leu4117Gln
|
|
XM_011530748.1:c.12350T>A
|
XP_011529050.1:p.Leu4117Gln
|
|
XM_011530749.1:c.12350T>A
|
XP_011529051.1:p.Leu4117Gln
|
|
XM_011530750.1:c.12350T>A
|
XP_011529052.1:p.Leu4117Gln
|
|
XM_011530751.1:c.12350T>A
|
XP_011529053.1:p.Leu4117Gln
|
|
XM_011530752.1:c.12347T>A
|
XP_011529054.1:p.Leu4116Gln
|
|
XM_011530753.1:c.12305T>A
|
XP_011529055.1:p.Leu4102Gln
|
|
XM_011530754.1:c.12302T>A
|
XP_011529056.1:p.Leu4101Gln
|
|
XM_011530755.1:c.12299T>A
|
XP_011529057.1:p.Leu4100Gln
|
|
XM_011530756.1:c.12251T>A
|
XP_011529058.1:p.Leu4084Gln
|
|
XM_011530757.1:c.11948T>A
|
XP_011529059.1:p.Leu3983Gln
|
|
XM_005261965.4:c.12101T>A
|
XP_005262022.1:p.Leu4034Gln
|
|
XM_011530751.2:c.12350T>A
|
XP_011529053.1:p.Leu4117Gln
|
|
XM_017029191.1:c.12482T>A
|
XP_016884680.1:p.Leu4161Gln
|
|
XM_017029192.1:c.12479T>A
|
XP_016884681.1:p.Leu4160Gln
|
|
XM_017029193.1:c.12461T>A
|
XP_016884682.1:p.Leu4154Gln
|
|
XM_017029194.1:c.12437T>A
|
XP_016884683.1:p.Leu4146Gln
|
|
XM_017029195.1:c.12434T>A
|
XP_016884684.1:p.Leu4145Gln
|
|
XM_017029196.1:c.12431T>A
|
XP_016884685.1:p.Leu4144Gln
|
|
XM_017029197.1:c.12383T>A
|
XP_016884686.1:p.Leu4128Gln
|
|
XM_017029198.2:c.12371T>A
|
XP_016884687.1:p.Leu4124Gln
|
|
XM_017029199.1:c.12371T>A
|
XP_016884688.1:p.Leu4124Gln
|
|
XM_017029200.1:c.12371T>A
|
XP_016884689.1:p.Leu4124Gln
|
|
XM_017029201.1:c.12371T>A
|
XP_016884690.1:p.Leu4124Gln
|
|
XM_017029202.1:c.12371T>A
|
XP_016884691.1:p.Leu4124Gln
|
|
XM_017029203.1:c.12371T>A
|
XP_016884692.1:p.Leu4124Gln
|
|
XM_017029204.1:c.12233T>A
|
XP_016884693.1:p.Leu4078Gln
|
|
XM_017029206.1:c.12080T>A
|
XP_016884695.1:p.Leu4027Gln
|
|
XM_024452322.1:c.12350T>A
|
XP_024308090.1:p.Leu4117Gln
|
|
NM_031407.7:c.12101T>A
MANE Select
|
NP_113584.3:p.Leu4034Gln
|
|