ENST00000704099.1:c.12647T>G
|
ENSP00000515693.1:p.Phe4216Cys
|
|
ENST00000262854.11:c.12863T>G
MANE Select
|
ENSP00000262854.6:p.Phe4288Cys
|
|
ENST00000262854.10:c.12863T>G
|
ENSP00000262854.6:p.Phe4288Cys
|
|
ENST00000342160.7:c.12863T>G
|
ENSP00000340648.3:p.Phe4288Cys
|
|
ENST00000426907.5:c.3330T>G
|
|
|
ENST00000488459.1:n.176T>G
|
|
|
ENST00000612484.4:c.12836T>G
|
ENSP00000479451.1:p.Phe4279Cys
|
|
NM_031407.6:c.12863T>G
|
NP_113584.3:p.Phe4288Cys
|
|
XM_005261965.2:c.12863T>G
|
XP_005262022.1:p.Phe4288Cys
|
|
XM_011530746.1:c.13112T>G
|
XP_011529048.1:p.Phe4371Cys
|
|
XM_011530747.1:c.13112T>G
|
XP_011529049.1:p.Phe4371Cys
|
|
XM_011530748.1:c.13112T>G
|
XP_011529050.1:p.Phe4371Cys
|
|
XM_011530749.1:c.13112T>G
|
XP_011529051.1:p.Phe4371Cys
|
|
XM_011530750.1:c.13112T>G
|
XP_011529052.1:p.Phe4371Cys
|
|
XM_011530751.1:c.13112T>G
|
XP_011529053.1:p.Phe4371Cys
|
|
XM_011530752.1:c.13109T>G
|
XP_011529054.1:p.Phe4370Cys
|
|
XM_011530753.1:c.13067T>G
|
XP_011529055.1:p.Phe4356Cys
|
|
XM_011530754.1:c.13064T>G
|
XP_011529056.1:p.Phe4355Cys
|
|
XM_011530755.1:c.13061T>G
|
XP_011529057.1:p.Phe4354Cys
|
|
XM_011530756.1:c.13013T>G
|
XP_011529058.1:p.Phe4338Cys
|
|
XM_011530757.1:c.12710T>G
|
XP_011529059.1:p.Phe4237Cys
|
|
XM_005261965.4:c.12863T>G
|
XP_005262022.1:p.Phe4288Cys
|
|
XM_011530751.2:c.13112T>G
|
XP_011529053.1:p.Phe4371Cys
|
|
XM_017029191.1:c.13244T>G
|
XP_016884680.1:p.Phe4415Cys
|
|
XM_017029192.1:c.13241T>G
|
XP_016884681.1:p.Phe4414Cys
|
|
XM_017029193.1:c.13223T>G
|
XP_016884682.1:p.Phe4408Cys
|
|
XM_017029194.1:c.13199T>G
|
XP_016884683.1:p.Phe4400Cys
|
|
XM_017029195.1:c.13196T>G
|
XP_016884684.1:p.Phe4399Cys
|
|
XM_017029196.1:c.13193T>G
|
XP_016884685.1:p.Phe4398Cys
|
|
XM_017029197.1:c.13145T>G
|
XP_016884686.1:p.Phe4382Cys
|
|
XM_017029198.2:c.13133T>G
|
XP_016884687.1:p.Phe4378Cys
|
|
XM_017029199.1:c.13133T>G
|
XP_016884688.1:p.Phe4378Cys
|
|
XM_017029200.1:c.13133T>G
|
XP_016884689.1:p.Phe4378Cys
|
|
XM_017029201.1:c.13133T>G
|
XP_016884690.1:p.Phe4378Cys
|
|
XM_017029202.1:c.13133T>G
|
XP_016884691.1:p.Phe4378Cys
|
|
XM_017029203.1:c.13133T>G
|
XP_016884692.1:p.Phe4378Cys
|
|
XM_017029204.1:c.12995T>G
|
XP_016884693.1:p.Phe4332Cys
|
|
XM_017029206.1:c.12842T>G
|
XP_016884695.1:p.Phe4281Cys
|
|
XM_024452322.1:c.13112T>G
|
XP_024308090.1:p.Phe4371Cys
|
|
NM_031407.7:c.12863T>G
MANE Select
|
NP_113584.3:p.Phe4288Cys
|
|