ENST00000704099.1:c.12805T>C
|
ENSP00000515693.1:p.Cys4269Arg
|
|
ENST00000262854.11:c.13021T>C
MANE Select
|
ENSP00000262854.6:p.Cys4341Arg
|
|
ENST00000262854.10:c.13021T>C
|
ENSP00000262854.6:p.Cys4341Arg
|
|
ENST00000342160.7:c.13021T>C
|
ENSP00000340648.3:p.Cys4341Arg
|
|
ENST00000426907.5:c.3488T>C
|
|
|
ENST00000488459.1:n.334T>C
|
|
|
ENST00000612484.4:c.12994T>C
|
ENSP00000479451.1:p.Cys4332Arg
|
|
NM_031407.6:c.13021T>C
|
NP_113584.3:p.Cys4341Arg
|
|
XM_005261965.2:c.13021T>C
|
XP_005262022.1:p.Cys4341Arg
|
|
XM_011530746.1:c.13270T>C
|
XP_011529048.1:p.Cys4424Arg
|
|
XM_011530747.1:c.13270T>C
|
XP_011529049.1:p.Cys4424Arg
|
|
XM_011530748.1:c.13270T>C
|
XP_011529050.1:p.Cys4424Arg
|
|
XM_011530749.1:c.13270T>C
|
XP_011529051.1:p.Cys4424Arg
|
|
XM_011530750.1:c.13270T>C
|
XP_011529052.1:p.Cys4424Arg
|
|
XM_011530751.1:c.13270T>C
|
XP_011529053.1:p.Cys4424Arg
|
|
XM_011530752.1:c.13267T>C
|
XP_011529054.1:p.Cys4423Arg
|
|
XM_011530753.1:c.13225T>C
|
XP_011529055.1:p.Cys4409Arg
|
|
XM_011530754.1:c.13222T>C
|
XP_011529056.1:p.Cys4408Arg
|
|
XM_011530755.1:c.13219T>C
|
XP_011529057.1:p.Cys4407Arg
|
|
XM_011530756.1:c.13171T>C
|
XP_011529058.1:p.Cys4391Arg
|
|
XM_011530757.1:c.12868T>C
|
XP_011529059.1:p.Cys4290Arg
|
|
XM_005261965.4:c.13021T>C
|
XP_005262022.1:p.Cys4341Arg
|
|
XM_011530751.2:c.13270T>C
|
XP_011529053.1:p.Cys4424Arg
|
|
XM_017029191.1:c.13402T>C
|
XP_016884680.1:p.Cys4468Arg
|
|
XM_017029192.1:c.13399T>C
|
XP_016884681.1:p.Cys4467Arg
|
|
XM_017029193.1:c.13381T>C
|
XP_016884682.1:p.Cys4461Arg
|
|
XM_017029194.1:c.13357T>C
|
XP_016884683.1:p.Cys4453Arg
|
|
XM_017029195.1:c.13354T>C
|
XP_016884684.1:p.Cys4452Arg
|
|
XM_017029196.1:c.13351T>C
|
XP_016884685.1:p.Cys4451Arg
|
|
XM_017029197.1:c.13303T>C
|
XP_016884686.1:p.Cys4435Arg
|
|
XM_017029198.2:c.13291T>C
|
XP_016884687.1:p.Cys4431Arg
|
|
XM_017029199.1:c.13291T>C
|
XP_016884688.1:p.Cys4431Arg
|
|
XM_017029200.1:c.13291T>C
|
XP_016884689.1:p.Cys4431Arg
|
|
XM_017029201.1:c.13291T>C
|
XP_016884690.1:p.Cys4431Arg
|
|
XM_017029202.1:c.13291T>C
|
XP_016884691.1:p.Cys4431Arg
|
|
XM_017029203.1:c.13291T>C
|
XP_016884692.1:p.Cys4431Arg
|
|
XM_017029204.1:c.13153T>C
|
XP_016884693.1:p.Cys4385Arg
|
|
XM_017029206.1:c.13000T>C
|
XP_016884695.1:p.Cys4334Arg
|
|
XM_024452322.1:c.13270T>C
|
XP_024308090.1:p.Cys4424Arg
|
|
NM_031407.7:c.13021T>C
MANE Select
|
NP_113584.3:p.Cys4341Arg
|
|