ENST00000704099.1:c.12769G>T
|
ENSP00000515693.1:p.Asp4257Tyr
|
|
ENST00000262854.11:c.12985G>T
MANE Select
|
ENSP00000262854.6:p.Asp4329Tyr
|
|
ENST00000262854.10:c.12985G>T
|
ENSP00000262854.6:p.Asp4329Tyr
|
|
ENST00000342160.7:c.12985G>T
|
ENSP00000340648.3:p.Asp4329Tyr
|
|
ENST00000426907.5:c.3452G>T
|
|
|
ENST00000488459.1:n.298G>T
|
|
|
ENST00000612484.4:c.12958G>T
|
ENSP00000479451.1:p.Asp4320Tyr
|
|
NM_031407.6:c.12985G>T
|
NP_113584.3:p.Asp4329Tyr
|
|
XM_005261965.2:c.12985G>T
|
XP_005262022.1:p.Asp4329Tyr
|
|
XM_011530746.1:c.13234G>T
|
XP_011529048.1:p.Asp4412Tyr
|
|
XM_011530747.1:c.13234G>T
|
XP_011529049.1:p.Asp4412Tyr
|
|
XM_011530748.1:c.13234G>T
|
XP_011529050.1:p.Asp4412Tyr
|
|
XM_011530749.1:c.13234G>T
|
XP_011529051.1:p.Asp4412Tyr
|
|
XM_011530750.1:c.13234G>T
|
XP_011529052.1:p.Asp4412Tyr
|
|
XM_011530751.1:c.13234G>T
|
XP_011529053.1:p.Asp4412Tyr
|
|
XM_011530752.1:c.13231G>T
|
XP_011529054.1:p.Asp4411Tyr
|
|
XM_011530753.1:c.13189G>T
|
XP_011529055.1:p.Asp4397Tyr
|
|
XM_011530754.1:c.13186G>T
|
XP_011529056.1:p.Asp4396Tyr
|
|
XM_011530755.1:c.13183G>T
|
XP_011529057.1:p.Asp4395Tyr
|
|
XM_011530756.1:c.13135G>T
|
XP_011529058.1:p.Asp4379Tyr
|
|
XM_011530757.1:c.12832G>T
|
XP_011529059.1:p.Asp4278Tyr
|
|
XM_005261965.4:c.12985G>T
|
XP_005262022.1:p.Asp4329Tyr
|
|
XM_011530751.2:c.13234G>T
|
XP_011529053.1:p.Asp4412Tyr
|
|
XM_017029191.1:c.13366G>T
|
XP_016884680.1:p.Asp4456Tyr
|
|
XM_017029192.1:c.13363G>T
|
XP_016884681.1:p.Asp4455Tyr
|
|
XM_017029193.1:c.13345G>T
|
XP_016884682.1:p.Asp4449Tyr
|
|
XM_017029194.1:c.13321G>T
|
XP_016884683.1:p.Asp4441Tyr
|
|
XM_017029195.1:c.13318G>T
|
XP_016884684.1:p.Asp4440Tyr
|
|
XM_017029196.1:c.13315G>T
|
XP_016884685.1:p.Asp4439Tyr
|
|
XM_017029197.1:c.13267G>T
|
XP_016884686.1:p.Asp4423Tyr
|
|
XM_017029198.2:c.13255G>T
|
XP_016884687.1:p.Asp4419Tyr
|
|
XM_017029199.1:c.13255G>T
|
XP_016884688.1:p.Asp4419Tyr
|
|
XM_017029200.1:c.13255G>T
|
XP_016884689.1:p.Asp4419Tyr
|
|
XM_017029201.1:c.13255G>T
|
XP_016884690.1:p.Asp4419Tyr
|
|
XM_017029202.1:c.13255G>T
|
XP_016884691.1:p.Asp4419Tyr
|
|
XM_017029203.1:c.13255G>T
|
XP_016884692.1:p.Asp4419Tyr
|
|
XM_017029204.1:c.13117G>T
|
XP_016884693.1:p.Asp4373Tyr
|
|
XM_017029206.1:c.12964G>T
|
XP_016884695.1:p.Asp4322Tyr
|
|
XM_024452322.1:c.13234G>T
|
XP_024308090.1:p.Asp4412Tyr
|
|
NM_031407.7:c.12985G>T
MANE Select
|
NP_113584.3:p.Asp4329Tyr
|
|