ENST00000704099.1:c.12634G=
|
ENSP00000515693.1:p.Ala4212=
|
|
ENST00000262854.11:c.12850G=
MANE Select
|
ENSP00000262854.6:p.Ala4284=
|
|
ENST00000262854.10:c.12850G=
|
ENSP00000262854.6:p.Ala4284=
|
|
ENST00000342160.7:c.12850G=
|
ENSP00000340648.3:p.Ala4284=
|
|
ENST00000426907.5:c.3317G=
|
|
|
ENST00000488459.1:n.163G=
|
|
|
ENST00000612484.4:c.12823G=
|
ENSP00000479451.1:p.Ala4275=
|
|
NM_031407.6:c.12850G=
|
NP_113584.3:p.Ala4284=
|
|
XM_005261965.2:c.12850G=
|
XP_005262022.1:p.Ala4284=
|
|
XM_011530746.1:c.13099G=
|
XP_011529048.1:p.Ala4367=
|
|
XM_011530747.1:c.13099G=
|
XP_011529049.1:p.Ala4367=
|
|
XM_011530748.1:c.13099G=
|
XP_011529050.1:p.Ala4367=
|
|
XM_011530749.1:c.13099G=
|
XP_011529051.1:p.Ala4367=
|
|
XM_011530750.1:c.13099G=
|
XP_011529052.1:p.Ala4367=
|
|
XM_011530751.1:c.13099G=
|
XP_011529053.1:p.Ala4367=
|
|
XM_011530752.1:c.13096G=
|
XP_011529054.1:p.Ala4366=
|
|
XM_011530753.1:c.13054G=
|
XP_011529055.1:p.Ala4352=
|
|
XM_011530754.1:c.13051G=
|
XP_011529056.1:p.Ala4351=
|
|
XM_011530755.1:c.13048G=
|
XP_011529057.1:p.Ala4350=
|
|
XM_011530756.1:c.13000G=
|
XP_011529058.1:p.Ala4334=
|
|
XM_011530757.1:c.12697G=
|
XP_011529059.1:p.Ala4233=
|
|
XM_005261965.4:c.12850G=
|
XP_005262022.1:p.Ala4284=
|
|
XM_011530751.2:c.13099G=
|
XP_011529053.1:p.Ala4367=
|
|
XM_017029191.1:c.13231G=
|
XP_016884680.1:p.Ala4411=
|
|
XM_017029192.1:c.13228G=
|
XP_016884681.1:p.Ala4410=
|
|
XM_017029193.1:c.13210G=
|
XP_016884682.1:p.Ala4404=
|
|
XM_017029194.1:c.13186G=
|
XP_016884683.1:p.Ala4396=
|
|
XM_017029195.1:c.13183G=
|
XP_016884684.1:p.Ala4395=
|
|
XM_017029196.1:c.13180G=
|
XP_016884685.1:p.Ala4394=
|
|
XM_017029197.1:c.13132G=
|
XP_016884686.1:p.Ala4378=
|
|
XM_017029198.2:c.13120G=
|
XP_016884687.1:p.Ala4374=
|
|
XM_017029199.1:c.13120G=
|
XP_016884688.1:p.Ala4374=
|
|
XM_017029200.1:c.13120G=
|
XP_016884689.1:p.Ala4374=
|
|
XM_017029201.1:c.13120G=
|
XP_016884690.1:p.Ala4374=
|
|
XM_017029202.1:c.13120G=
|
XP_016884691.1:p.Ala4374=
|
|
XM_017029203.1:c.13120G=
|
XP_016884692.1:p.Ala4374=
|
|
XM_017029204.1:c.12982G=
|
XP_016884693.1:p.Ala4328=
|
|
XM_017029206.1:c.12829G=
|
XP_016884695.1:p.Ala4277=
|
|
XM_024452322.1:c.13099G=
|
XP_024308090.1:p.Ala4367=
|
|
NM_031407.7:c.12850G=
MANE Select
|
NP_113584.3:p.Ala4284=
|
|