ENST00000704099.1:c.12652C>A
|
ENSP00000515693.1:p.Gln4218Lys
|
|
ENST00000262854.11:c.12868C>A
MANE Select
|
ENSP00000262854.6:p.Gln4290Lys
|
|
ENST00000262854.10:c.12868C>A
|
ENSP00000262854.6:p.Gln4290Lys
|
|
ENST00000342160.7:c.12868C>A
|
ENSP00000340648.3:p.Gln4290Lys
|
|
ENST00000426907.5:c.3335C>A
|
|
|
ENST00000488459.1:n.181C>A
|
|
|
ENST00000612484.4:c.12841C>A
|
ENSP00000479451.1:p.Gln4281Lys
|
|
NM_031407.6:c.12868C>A
|
NP_113584.3:p.Gln4290Lys
|
|
XM_005261965.2:c.12868C>A
|
XP_005262022.1:p.Gln4290Lys
|
|
XM_011530746.1:c.13117C>A
|
XP_011529048.1:p.Gln4373Lys
|
|
XM_011530747.1:c.13117C>A
|
XP_011529049.1:p.Gln4373Lys
|
|
XM_011530748.1:c.13117C>A
|
XP_011529050.1:p.Gln4373Lys
|
|
XM_011530749.1:c.13117C>A
|
XP_011529051.1:p.Gln4373Lys
|
|
XM_011530750.1:c.13117C>A
|
XP_011529052.1:p.Gln4373Lys
|
|
XM_011530751.1:c.13117C>A
|
XP_011529053.1:p.Gln4373Lys
|
|
XM_011530752.1:c.13114C>A
|
XP_011529054.1:p.Gln4372Lys
|
|
XM_011530753.1:c.13072C>A
|
XP_011529055.1:p.Gln4358Lys
|
|
XM_011530754.1:c.13069C>A
|
XP_011529056.1:p.Gln4357Lys
|
|
XM_011530755.1:c.13066C>A
|
XP_011529057.1:p.Gln4356Lys
|
|
XM_011530756.1:c.13018C>A
|
XP_011529058.1:p.Gln4340Lys
|
|
XM_011530757.1:c.12715C>A
|
XP_011529059.1:p.Gln4239Lys
|
|
XM_005261965.4:c.12868C>A
|
XP_005262022.1:p.Gln4290Lys
|
|
XM_011530751.2:c.13117C>A
|
XP_011529053.1:p.Gln4373Lys
|
|
XM_017029191.1:c.13249C>A
|
XP_016884680.1:p.Gln4417Lys
|
|
XM_017029192.1:c.13246C>A
|
XP_016884681.1:p.Gln4416Lys
|
|
XM_017029193.1:c.13228C>A
|
XP_016884682.1:p.Gln4410Lys
|
|
XM_017029194.1:c.13204C>A
|
XP_016884683.1:p.Gln4402Lys
|
|
XM_017029195.1:c.13201C>A
|
XP_016884684.1:p.Gln4401Lys
|
|
XM_017029196.1:c.13198C>A
|
XP_016884685.1:p.Gln4400Lys
|
|
XM_017029197.1:c.13150C>A
|
XP_016884686.1:p.Gln4384Lys
|
|
XM_017029198.2:c.13138C>A
|
XP_016884687.1:p.Gln4380Lys
|
|
XM_017029199.1:c.13138C>A
|
XP_016884688.1:p.Gln4380Lys
|
|
XM_017029200.1:c.13138C>A
|
XP_016884689.1:p.Gln4380Lys
|
|
XM_017029201.1:c.13138C>A
|
XP_016884690.1:p.Gln4380Lys
|
|
XM_017029202.1:c.13138C>A
|
XP_016884691.1:p.Gln4380Lys
|
|
XM_017029203.1:c.13138C>A
|
XP_016884692.1:p.Gln4380Lys
|
|
XM_017029204.1:c.13000C>A
|
XP_016884693.1:p.Gln4334Lys
|
|
XM_017029206.1:c.12847C>A
|
XP_016884695.1:p.Gln4283Lys
|
|
XM_024452322.1:c.13117C>A
|
XP_024308090.1:p.Gln4373Lys
|
|
NM_031407.7:c.12868C>A
MANE Select
|
NP_113584.3:p.Gln4290Lys
|
|