ENST00000704099.1:c.12620A>G
|
ENSP00000515693.1:p.Gln4207Arg
|
|
ENST00000262854.11:c.12836A>G
MANE Select
|
ENSP00000262854.6:p.Gln4279Arg
|
|
ENST00000262854.10:c.12836A>G
|
ENSP00000262854.6:p.Gln4279Arg
|
|
ENST00000342160.7:c.12836A>G
|
ENSP00000340648.3:p.Gln4279Arg
|
|
ENST00000426907.5:c.3303A>G
|
|
|
ENST00000488459.1:n.149A>G
|
|
|
ENST00000612484.4:c.12809A>G
|
ENSP00000479451.1:p.Gln4270Arg
|
|
NM_031407.6:c.12836A>G
|
NP_113584.3:p.Gln4279Arg
|
|
XM_005261965.2:c.12836A>G
|
XP_005262022.1:p.Gln4279Arg
|
|
XM_011530746.1:c.13085A>G
|
XP_011529048.1:p.Gln4362Arg
|
|
XM_011530747.1:c.13085A>G
|
XP_011529049.1:p.Gln4362Arg
|
|
XM_011530748.1:c.13085A>G
|
XP_011529050.1:p.Gln4362Arg
|
|
XM_011530749.1:c.13085A>G
|
XP_011529051.1:p.Gln4362Arg
|
|
XM_011530750.1:c.13085A>G
|
XP_011529052.1:p.Gln4362Arg
|
|
XM_011530751.1:c.13085A>G
|
XP_011529053.1:p.Gln4362Arg
|
|
XM_011530752.1:c.13082A>G
|
XP_011529054.1:p.Gln4361Arg
|
|
XM_011530753.1:c.13040A>G
|
XP_011529055.1:p.Gln4347Arg
|
|
XM_011530754.1:c.13037A>G
|
XP_011529056.1:p.Gln4346Arg
|
|
XM_011530755.1:c.13034A>G
|
XP_011529057.1:p.Gln4345Arg
|
|
XM_011530756.1:c.12986A>G
|
XP_011529058.1:p.Gln4329Arg
|
|
XM_011530757.1:c.12683A>G
|
XP_011529059.1:p.Gln4228Arg
|
|
XM_005261965.4:c.12836A>G
|
XP_005262022.1:p.Gln4279Arg
|
|
XM_011530751.2:c.13085A>G
|
XP_011529053.1:p.Gln4362Arg
|
|
XM_017029191.1:c.13217A>G
|
XP_016884680.1:p.Gln4406Arg
|
|
XM_017029192.1:c.13214A>G
|
XP_016884681.1:p.Gln4405Arg
|
|
XM_017029193.1:c.13196A>G
|
XP_016884682.1:p.Gln4399Arg
|
|
XM_017029194.1:c.13172A>G
|
XP_016884683.1:p.Gln4391Arg
|
|
XM_017029195.1:c.13169A>G
|
XP_016884684.1:p.Gln4390Arg
|
|
XM_017029196.1:c.13166A>G
|
XP_016884685.1:p.Gln4389Arg
|
|
XM_017029197.1:c.13118A>G
|
XP_016884686.1:p.Gln4373Arg
|
|
XM_017029198.2:c.13106A>G
|
XP_016884687.1:p.Gln4369Arg
|
|
XM_017029199.1:c.13106A>G
|
XP_016884688.1:p.Gln4369Arg
|
|
XM_017029200.1:c.13106A>G
|
XP_016884689.1:p.Gln4369Arg
|
|
XM_017029201.1:c.13106A>G
|
XP_016884690.1:p.Gln4369Arg
|
|
XM_017029202.1:c.13106A>G
|
XP_016884691.1:p.Gln4369Arg
|
|
XM_017029203.1:c.13106A>G
|
XP_016884692.1:p.Gln4369Arg
|
|
XM_017029204.1:c.12968A>G
|
XP_016884693.1:p.Gln4323Arg
|
|
XM_017029206.1:c.12815A>G
|
XP_016884695.1:p.Gln4272Arg
|
|
XM_024452322.1:c.13085A>G
|
XP_024308090.1:p.Gln4362Arg
|
|
NM_031407.7:c.12836A>G
MANE Select
|
NP_113584.3:p.Gln4279Arg
|
|