ENST00000704099.1:c.11803C>G
|
ENSP00000515693.1:p.Arg3935Gly
|
|
ENST00000262854.11:c.12019C>G
MANE Select
|
ENSP00000262854.6:p.Arg4007Gly
|
|
ENST00000262854.10:c.12019C>G
|
ENSP00000262854.6:p.Arg4007Gly
|
|
ENST00000342160.7:c.12019C>G
|
ENSP00000340648.3:p.Arg4007Gly
|
|
ENST00000426907.5:c.2486C>G
|
|
|
ENST00000480438.1:n.154C>G
|
|
|
ENST00000612484.4:c.11992C>G
|
ENSP00000479451.1:p.Arg3998Gly
|
|
NM_031407.6:c.12019C>G
|
NP_113584.3:p.Arg4007Gly
|
|
XM_005261965.2:c.12019C>G
|
XP_005262022.1:p.Arg4007Gly
|
|
XM_011530746.1:c.12268C>G
|
XP_011529048.1:p.Arg4090Gly
|
|
XM_011530747.1:c.12268C>G
|
XP_011529049.1:p.Arg4090Gly
|
|
XM_011530748.1:c.12268C>G
|
XP_011529050.1:p.Arg4090Gly
|
|
XM_011530749.1:c.12268C>G
|
XP_011529051.1:p.Arg4090Gly
|
|
XM_011530750.1:c.12268C>G
|
XP_011529052.1:p.Arg4090Gly
|
|
XM_011530751.1:c.12268C>G
|
XP_011529053.1:p.Arg4090Gly
|
|
XM_011530752.1:c.12265C>G
|
XP_011529054.1:p.Arg4089Gly
|
|
XM_011530753.1:c.12223C>G
|
XP_011529055.1:p.Arg4075Gly
|
|
XM_011530754.1:c.12220C>G
|
XP_011529056.1:p.Arg4074Gly
|
|
XM_011530755.1:c.12217C>G
|
XP_011529057.1:p.Arg4073Gly
|
|
XM_011530756.1:c.12169C>G
|
XP_011529058.1:p.Arg4057Gly
|
|
XM_011530757.1:c.11866C>G
|
XP_011529059.1:p.Arg3956Gly
|
|
XM_005261965.4:c.12019C>G
|
XP_005262022.1:p.Arg4007Gly
|
|
XM_011530751.2:c.12268C>G
|
XP_011529053.1:p.Arg4090Gly
|
|
XM_017029191.1:c.12400C>G
|
XP_016884680.1:p.Arg4134Gly
|
|
XM_017029192.1:c.12397C>G
|
XP_016884681.1:p.Arg4133Gly
|
|
XM_017029193.1:c.12379C>G
|
XP_016884682.1:p.Arg4127Gly
|
|
XM_017029194.1:c.12355C>G
|
XP_016884683.1:p.Arg4119Gly
|
|
XM_017029195.1:c.12352C>G
|
XP_016884684.1:p.Arg4118Gly
|
|
XM_017029196.1:c.12349C>G
|
XP_016884685.1:p.Arg4117Gly
|
|
XM_017029197.1:c.12301C>G
|
XP_016884686.1:p.Arg4101Gly
|
|
XM_017029198.2:c.12289C>G
|
XP_016884687.1:p.Arg4097Gly
|
|
XM_017029199.1:c.12289C>G
|
XP_016884688.1:p.Arg4097Gly
|
|
XM_017029200.1:c.12289C>G
|
XP_016884689.1:p.Arg4097Gly
|
|
XM_017029201.1:c.12289C>G
|
XP_016884690.1:p.Arg4097Gly
|
|
XM_017029202.1:c.12289C>G
|
XP_016884691.1:p.Arg4097Gly
|
|
XM_017029203.1:c.12289C>G
|
XP_016884692.1:p.Arg4097Gly
|
|
XM_017029204.1:c.12151C>G
|
XP_016884693.1:p.Arg4051Gly
|
|
XM_017029206.1:c.11998C>G
|
XP_016884695.1:p.Arg4000Gly
|
|
XM_024452322.1:c.12268C>G
|
XP_024308090.1:p.Arg4090Gly
|
|
NM_031407.7:c.12019C>G
MANE Select
|
NP_113584.3:p.Arg4007Gly
|
|