ENST00000704099.1:c.11871C=
|
ENSP00000515693.1:p.Asp3957=
|
|
ENST00000262854.11:c.12087C=
MANE Select
|
ENSP00000262854.6:p.Asp4029=
|
|
ENST00000262854.10:c.12087C=
|
ENSP00000262854.6:p.Asp4029=
|
|
ENST00000342160.7:c.12087C=
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ENSP00000340648.3:p.Asp4029=
|
|
ENST00000426907.5:c.2554C=
|
|
|
ENST00000480438.1:n.222C=
|
|
|
ENST00000612484.4:c.12060C=
|
ENSP00000479451.1:p.Asp4020=
|
|
NM_031407.6:c.12087C=
|
NP_113584.3:p.Asp4029=
|
|
XM_005261965.2:c.12087C=
|
XP_005262022.1:p.Asp4029=
|
|
XM_011530746.1:c.12336C=
|
XP_011529048.1:p.Asp4112=
|
|
XM_011530747.1:c.12336C=
|
XP_011529049.1:p.Asp4112=
|
|
XM_011530748.1:c.12336C=
|
XP_011529050.1:p.Asp4112=
|
|
XM_011530749.1:c.12336C=
|
XP_011529051.1:p.Asp4112=
|
|
XM_011530750.1:c.12336C=
|
XP_011529052.1:p.Asp4112=
|
|
XM_011530751.1:c.12336C=
|
XP_011529053.1:p.Asp4112=
|
|
XM_011530752.1:c.12333C=
|
XP_011529054.1:p.Asp4111=
|
|
XM_011530753.1:c.12291C=
|
XP_011529055.1:p.Asp4097=
|
|
XM_011530754.1:c.12288C=
|
XP_011529056.1:p.Asp4096=
|
|
XM_011530755.1:c.12285C=
|
XP_011529057.1:p.Asp4095=
|
|
XM_011530756.1:c.12237C=
|
XP_011529058.1:p.Asp4079=
|
|
XM_011530757.1:c.11934C=
|
XP_011529059.1:p.Asp3978=
|
|
XM_005261965.4:c.12087C=
|
XP_005262022.1:p.Asp4029=
|
|
XM_011530751.2:c.12336C=
|
XP_011529053.1:p.Asp4112=
|
|
XM_017029191.1:c.12468C=
|
XP_016884680.1:p.Asp4156=
|
|
XM_017029192.1:c.12465C=
|
XP_016884681.1:p.Asp4155=
|
|
XM_017029193.1:c.12447C=
|
XP_016884682.1:p.Asp4149=
|
|
XM_017029194.1:c.12423C=
|
XP_016884683.1:p.Asp4141=
|
|
XM_017029195.1:c.12420C=
|
XP_016884684.1:p.Asp4140=
|
|
XM_017029196.1:c.12417C=
|
XP_016884685.1:p.Asp4139=
|
|
XM_017029197.1:c.12369C=
|
XP_016884686.1:p.Asp4123=
|
|
XM_017029198.2:c.12357C=
|
XP_016884687.1:p.Asp4119=
|
|
XM_017029199.1:c.12357C=
|
XP_016884688.1:p.Asp4119=
|
|
XM_017029200.1:c.12357C=
|
XP_016884689.1:p.Asp4119=
|
|
XM_017029201.1:c.12357C=
|
XP_016884690.1:p.Asp4119=
|
|
XM_017029202.1:c.12357C=
|
XP_016884691.1:p.Asp4119=
|
|
XM_017029203.1:c.12357C=
|
XP_016884692.1:p.Asp4119=
|
|
XM_017029204.1:c.12219C=
|
XP_016884693.1:p.Asp4073=
|
|
XM_017029206.1:c.12066C=
|
XP_016884695.1:p.Asp4022=
|
|
XM_024452322.1:c.12336C=
|
XP_024308090.1:p.Asp4112=
|
|
NM_031407.7:c.12087C=
MANE Select
|
NP_113584.3:p.Asp4029=
|
|