ENST00000704099.1:c.11892C>G
|
ENSP00000515693.1:p.Arg3964=
|
|
ENST00000262854.11:c.12108C>G
MANE Select
|
ENSP00000262854.6:p.Arg4036=
|
|
ENST00000262854.10:c.12108C>G
|
ENSP00000262854.6:p.Arg4036=
|
|
ENST00000342160.7:c.12108C>G
|
ENSP00000340648.3:p.Arg4036=
|
|
ENST00000426907.5:c.2575C>G
|
|
|
ENST00000480438.1:n.243C>G
|
|
|
ENST00000612484.4:c.12081C>G
|
ENSP00000479451.1:p.Arg4027=
|
|
NM_031407.6:c.12108C>G
|
NP_113584.3:p.Arg4036=
|
|
XM_005261965.2:c.12108C>G
|
XP_005262022.1:p.Arg4036=
|
|
XM_011530746.1:c.12357C>G
|
XP_011529048.1:p.Arg4119=
|
|
XM_011530747.1:c.12357C>G
|
XP_011529049.1:p.Arg4119=
|
|
XM_011530748.1:c.12357C>G
|
XP_011529050.1:p.Arg4119=
|
|
XM_011530749.1:c.12357C>G
|
XP_011529051.1:p.Arg4119=
|
|
XM_011530750.1:c.12357C>G
|
XP_011529052.1:p.Arg4119=
|
|
XM_011530751.1:c.12357C>G
|
XP_011529053.1:p.Arg4119=
|
|
XM_011530752.1:c.12354C>G
|
XP_011529054.1:p.Arg4118=
|
|
XM_011530753.1:c.12312C>G
|
XP_011529055.1:p.Arg4104=
|
|
XM_011530754.1:c.12309C>G
|
XP_011529056.1:p.Arg4103=
|
|
XM_011530755.1:c.12306C>G
|
XP_011529057.1:p.Arg4102=
|
|
XM_011530756.1:c.12258C>G
|
XP_011529058.1:p.Arg4086=
|
|
XM_011530757.1:c.11955C>G
|
XP_011529059.1:p.Arg3985=
|
|
XM_005261965.4:c.12108C>G
|
XP_005262022.1:p.Arg4036=
|
|
XM_011530751.2:c.12357C>G
|
XP_011529053.1:p.Arg4119=
|
|
XM_017029191.1:c.12489C>G
|
XP_016884680.1:p.Arg4163=
|
|
XM_017029192.1:c.12486C>G
|
XP_016884681.1:p.Arg4162=
|
|
XM_017029193.1:c.12468C>G
|
XP_016884682.1:p.Arg4156=
|
|
XM_017029194.1:c.12444C>G
|
XP_016884683.1:p.Arg4148=
|
|
XM_017029195.1:c.12441C>G
|
XP_016884684.1:p.Arg4147=
|
|
XM_017029196.1:c.12438C>G
|
XP_016884685.1:p.Arg4146=
|
|
XM_017029197.1:c.12390C>G
|
XP_016884686.1:p.Arg4130=
|
|
XM_017029198.2:c.12378C>G
|
XP_016884687.1:p.Arg4126=
|
|
XM_017029199.1:c.12378C>G
|
XP_016884688.1:p.Arg4126=
|
|
XM_017029200.1:c.12378C>G
|
XP_016884689.1:p.Arg4126=
|
|
XM_017029201.1:c.12378C>G
|
XP_016884690.1:p.Arg4126=
|
|
XM_017029202.1:c.12378C>G
|
XP_016884691.1:p.Arg4126=
|
|
XM_017029203.1:c.12378C>G
|
XP_016884692.1:p.Arg4126=
|
|
XM_017029204.1:c.12240C>G
|
XP_016884693.1:p.Arg4080=
|
|
XM_017029206.1:c.12087C>G
|
XP_016884695.1:p.Arg4029=
|
|
XM_024452322.1:c.12357C>G
|
XP_024308090.1:p.Arg4119=
|
|
NM_031407.7:c.12108C>G
MANE Select
|
NP_113584.3:p.Arg4036=
|
|