ENST00000704099.1:c.12637T>G
|
ENSP00000515693.1:p.Leu4213Val
|
|
ENST00000262854.11:c.12853T>G
MANE Select
|
ENSP00000262854.6:p.Leu4285Val
|
|
ENST00000262854.10:c.12853T>G
|
ENSP00000262854.6:p.Leu4285Val
|
|
ENST00000342160.7:c.12853T>G
|
ENSP00000340648.3:p.Leu4285Val
|
|
ENST00000426907.5:c.3320T>G
|
|
|
ENST00000488459.1:n.166T>G
|
|
|
ENST00000612484.4:c.12826T>G
|
ENSP00000479451.1:p.Leu4276Val
|
|
NM_031407.6:c.12853T>G
|
NP_113584.3:p.Leu4285Val
|
|
XM_005261965.2:c.12853T>G
|
XP_005262022.1:p.Leu4285Val
|
|
XM_011530746.1:c.13102T>G
|
XP_011529048.1:p.Leu4368Val
|
|
XM_011530747.1:c.13102T>G
|
XP_011529049.1:p.Leu4368Val
|
|
XM_011530748.1:c.13102T>G
|
XP_011529050.1:p.Leu4368Val
|
|
XM_011530749.1:c.13102T>G
|
XP_011529051.1:p.Leu4368Val
|
|
XM_011530750.1:c.13102T>G
|
XP_011529052.1:p.Leu4368Val
|
|
XM_011530751.1:c.13102T>G
|
XP_011529053.1:p.Leu4368Val
|
|
XM_011530752.1:c.13099T>G
|
XP_011529054.1:p.Leu4367Val
|
|
XM_011530753.1:c.13057T>G
|
XP_011529055.1:p.Leu4353Val
|
|
XM_011530754.1:c.13054T>G
|
XP_011529056.1:p.Leu4352Val
|
|
XM_011530755.1:c.13051T>G
|
XP_011529057.1:p.Leu4351Val
|
|
XM_011530756.1:c.13003T>G
|
XP_011529058.1:p.Leu4335Val
|
|
XM_011530757.1:c.12700T>G
|
XP_011529059.1:p.Leu4234Val
|
|
XM_005261965.4:c.12853T>G
|
XP_005262022.1:p.Leu4285Val
|
|
XM_011530751.2:c.13102T>G
|
XP_011529053.1:p.Leu4368Val
|
|
XM_017029191.1:c.13234T>G
|
XP_016884680.1:p.Leu4412Val
|
|
XM_017029192.1:c.13231T>G
|
XP_016884681.1:p.Leu4411Val
|
|
XM_017029193.1:c.13213T>G
|
XP_016884682.1:p.Leu4405Val
|
|
XM_017029194.1:c.13189T>G
|
XP_016884683.1:p.Leu4397Val
|
|
XM_017029195.1:c.13186T>G
|
XP_016884684.1:p.Leu4396Val
|
|
XM_017029196.1:c.13183T>G
|
XP_016884685.1:p.Leu4395Val
|
|
XM_017029197.1:c.13135T>G
|
XP_016884686.1:p.Leu4379Val
|
|
XM_017029198.2:c.13123T>G
|
XP_016884687.1:p.Leu4375Val
|
|
XM_017029199.1:c.13123T>G
|
XP_016884688.1:p.Leu4375Val
|
|
XM_017029200.1:c.13123T>G
|
XP_016884689.1:p.Leu4375Val
|
|
XM_017029201.1:c.13123T>G
|
XP_016884690.1:p.Leu4375Val
|
|
XM_017029202.1:c.13123T>G
|
XP_016884691.1:p.Leu4375Val
|
|
XM_017029203.1:c.13123T>G
|
XP_016884692.1:p.Leu4375Val
|
|
XM_017029204.1:c.12985T>G
|
XP_016884693.1:p.Leu4329Val
|
|
XM_017029206.1:c.12832T>G
|
XP_016884695.1:p.Leu4278Val
|
|
XM_024452322.1:c.13102T>G
|
XP_024308090.1:p.Leu4368Val
|
|
NM_031407.7:c.12853T>G
MANE Select
|
NP_113584.3:p.Leu4285Val
|
|