ENST00000704099.1:c.12616A>G
|
ENSP00000515693.1:p.Ile4206Val
|
|
ENST00000262854.11:c.12832A>G
MANE Select
|
ENSP00000262854.6:p.Ile4278Val
|
|
ENST00000262854.10:c.12832A>G
|
ENSP00000262854.6:p.Ile4278Val
|
|
ENST00000342160.7:c.12832A>G
|
ENSP00000340648.3:p.Ile4278Val
|
|
ENST00000426907.5:c.3299A>G
|
|
|
ENST00000488459.1:n.145A>G
|
|
|
ENST00000612484.4:c.12805A>G
|
ENSP00000479451.1:p.Ile4269Val
|
|
NM_031407.6:c.12832A>G
|
NP_113584.3:p.Ile4278Val
|
|
XM_005261965.2:c.12832A>G
|
XP_005262022.1:p.Ile4278Val
|
|
XM_011530746.1:c.13081A>G
|
XP_011529048.1:p.Ile4361Val
|
|
XM_011530747.1:c.13081A>G
|
XP_011529049.1:p.Ile4361Val
|
|
XM_011530748.1:c.13081A>G
|
XP_011529050.1:p.Ile4361Val
|
|
XM_011530749.1:c.13081A>G
|
XP_011529051.1:p.Ile4361Val
|
|
XM_011530750.1:c.13081A>G
|
XP_011529052.1:p.Ile4361Val
|
|
XM_011530751.1:c.13081A>G
|
XP_011529053.1:p.Ile4361Val
|
|
XM_011530752.1:c.13078A>G
|
XP_011529054.1:p.Ile4360Val
|
|
XM_011530753.1:c.13036A>G
|
XP_011529055.1:p.Ile4346Val
|
|
XM_011530754.1:c.13033A>G
|
XP_011529056.1:p.Ile4345Val
|
|
XM_011530755.1:c.13030A>G
|
XP_011529057.1:p.Ile4344Val
|
|
XM_011530756.1:c.12982A>G
|
XP_011529058.1:p.Ile4328Val
|
|
XM_011530757.1:c.12679A>G
|
XP_011529059.1:p.Ile4227Val
|
|
XM_005261965.4:c.12832A>G
|
XP_005262022.1:p.Ile4278Val
|
|
XM_011530751.2:c.13081A>G
|
XP_011529053.1:p.Ile4361Val
|
|
XM_017029191.1:c.13213A>G
|
XP_016884680.1:p.Ile4405Val
|
|
XM_017029192.1:c.13210A>G
|
XP_016884681.1:p.Ile4404Val
|
|
XM_017029193.1:c.13192A>G
|
XP_016884682.1:p.Ile4398Val
|
|
XM_017029194.1:c.13168A>G
|
XP_016884683.1:p.Ile4390Val
|
|
XM_017029195.1:c.13165A>G
|
XP_016884684.1:p.Ile4389Val
|
|
XM_017029196.1:c.13162A>G
|
XP_016884685.1:p.Ile4388Val
|
|
XM_017029197.1:c.13114A>G
|
XP_016884686.1:p.Ile4372Val
|
|
XM_017029198.2:c.13102A>G
|
XP_016884687.1:p.Ile4368Val
|
|
XM_017029199.1:c.13102A>G
|
XP_016884688.1:p.Ile4368Val
|
|
XM_017029200.1:c.13102A>G
|
XP_016884689.1:p.Ile4368Val
|
|
XM_017029201.1:c.13102A>G
|
XP_016884690.1:p.Ile4368Val
|
|
XM_017029202.1:c.13102A>G
|
XP_016884691.1:p.Ile4368Val
|
|
XM_017029203.1:c.13102A>G
|
XP_016884692.1:p.Ile4368Val
|
|
XM_017029204.1:c.12964A>G
|
XP_016884693.1:p.Ile4322Val
|
|
XM_017029206.1:c.12811A>G
|
XP_016884695.1:p.Ile4271Val
|
|
XM_024452322.1:c.13081A>G
|
XP_024308090.1:p.Ile4361Val
|
|
NM_031407.7:c.12832A>G
MANE Select
|
NP_113584.3:p.Ile4278Val
|
|