ENST00000704099.1:c.11846T>G
|
ENSP00000515693.1:p.Val3949Gly
|
|
ENST00000262854.11:c.12062T>G
MANE Select
|
ENSP00000262854.6:p.Val4021Gly
|
|
ENST00000262854.10:c.12062T>G
|
ENSP00000262854.6:p.Val4021Gly
|
|
ENST00000342160.7:c.12062T>G
|
ENSP00000340648.3:p.Val4021Gly
|
|
ENST00000426907.5:c.2529T>G
|
|
|
ENST00000480438.1:n.197T>G
|
|
|
ENST00000612484.4:c.12035T>G
|
ENSP00000479451.1:p.Val4012Gly
|
|
NM_031407.6:c.12062T>G
|
NP_113584.3:p.Val4021Gly
|
|
XM_005261965.2:c.12062T>G
|
XP_005262022.1:p.Val4021Gly
|
|
XM_011530746.1:c.12311T>G
|
XP_011529048.1:p.Val4104Gly
|
|
XM_011530747.1:c.12311T>G
|
XP_011529049.1:p.Val4104Gly
|
|
XM_011530748.1:c.12311T>G
|
XP_011529050.1:p.Val4104Gly
|
|
XM_011530749.1:c.12311T>G
|
XP_011529051.1:p.Val4104Gly
|
|
XM_011530750.1:c.12311T>G
|
XP_011529052.1:p.Val4104Gly
|
|
XM_011530751.1:c.12311T>G
|
XP_011529053.1:p.Val4104Gly
|
|
XM_011530752.1:c.12308T>G
|
XP_011529054.1:p.Val4103Gly
|
|
XM_011530753.1:c.12266T>G
|
XP_011529055.1:p.Val4089Gly
|
|
XM_011530754.1:c.12263T>G
|
XP_011529056.1:p.Val4088Gly
|
|
XM_011530755.1:c.12260T>G
|
XP_011529057.1:p.Val4087Gly
|
|
XM_011530756.1:c.12212T>G
|
XP_011529058.1:p.Val4071Gly
|
|
XM_011530757.1:c.11909T>G
|
XP_011529059.1:p.Val3970Gly
|
|
XM_005261965.4:c.12062T>G
|
XP_005262022.1:p.Val4021Gly
|
|
XM_011530751.2:c.12311T>G
|
XP_011529053.1:p.Val4104Gly
|
|
XM_017029191.1:c.12443T>G
|
XP_016884680.1:p.Val4148Gly
|
|
XM_017029192.1:c.12440T>G
|
XP_016884681.1:p.Val4147Gly
|
|
XM_017029193.1:c.12422T>G
|
XP_016884682.1:p.Val4141Gly
|
|
XM_017029194.1:c.12398T>G
|
XP_016884683.1:p.Val4133Gly
|
|
XM_017029195.1:c.12395T>G
|
XP_016884684.1:p.Val4132Gly
|
|
XM_017029196.1:c.12392T>G
|
XP_016884685.1:p.Val4131Gly
|
|
XM_017029197.1:c.12344T>G
|
XP_016884686.1:p.Val4115Gly
|
|
XM_017029198.2:c.12332T>G
|
XP_016884687.1:p.Val4111Gly
|
|
XM_017029199.1:c.12332T>G
|
XP_016884688.1:p.Val4111Gly
|
|
XM_017029200.1:c.12332T>G
|
XP_016884689.1:p.Val4111Gly
|
|
XM_017029201.1:c.12332T>G
|
XP_016884690.1:p.Val4111Gly
|
|
XM_017029202.1:c.12332T>G
|
XP_016884691.1:p.Val4111Gly
|
|
XM_017029203.1:c.12332T>G
|
XP_016884692.1:p.Val4111Gly
|
|
XM_017029204.1:c.12194T>G
|
XP_016884693.1:p.Val4065Gly
|
|
XM_017029206.1:c.12041T>G
|
XP_016884695.1:p.Val4014Gly
|
|
XM_024452322.1:c.12311T>G
|
XP_024308090.1:p.Val4104Gly
|
|
NM_031407.7:c.12062T>G
MANE Select
|
NP_113584.3:p.Val4021Gly
|
|