ENST00000704099.1:c.12801C>T
|
ENSP00000515693.1:p.His4267=
|
|
ENST00000262854.11:c.13017C>T
MANE Select
|
ENSP00000262854.6:p.His4339=
|
|
ENST00000262854.10:c.13017C>T
|
ENSP00000262854.6:p.His4339=
|
|
ENST00000342160.7:c.13017C>T
|
ENSP00000340648.3:p.His4339=
|
|
ENST00000426907.5:c.3484C>T
|
|
|
ENST00000488459.1:n.330C>T
|
|
|
ENST00000612484.4:c.12990C>T
|
ENSP00000479451.1:p.His4330=
|
|
NM_031407.6:c.13017C>T
|
NP_113584.3:p.His4339=
|
|
XM_005261965.2:c.13017C>T
|
XP_005262022.1:p.His4339=
|
|
XM_011530746.1:c.13266C>T
|
XP_011529048.1:p.His4422=
|
|
XM_011530747.1:c.13266C>T
|
XP_011529049.1:p.His4422=
|
|
XM_011530748.1:c.13266C>T
|
XP_011529050.1:p.His4422=
|
|
XM_011530749.1:c.13266C>T
|
XP_011529051.1:p.His4422=
|
|
XM_011530750.1:c.13266C>T
|
XP_011529052.1:p.His4422=
|
|
XM_011530751.1:c.13266C>T
|
XP_011529053.1:p.His4422=
|
|
XM_011530752.1:c.13263C>T
|
XP_011529054.1:p.His4421=
|
|
XM_011530753.1:c.13221C>T
|
XP_011529055.1:p.His4407=
|
|
XM_011530754.1:c.13218C>T
|
XP_011529056.1:p.His4406=
|
|
XM_011530755.1:c.13215C>T
|
XP_011529057.1:p.His4405=
|
|
XM_011530756.1:c.13167C>T
|
XP_011529058.1:p.His4389=
|
|
XM_011530757.1:c.12864C>T
|
XP_011529059.1:p.His4288=
|
|
XM_005261965.4:c.13017C>T
|
XP_005262022.1:p.His4339=
|
|
XM_011530751.2:c.13266C>T
|
XP_011529053.1:p.His4422=
|
|
XM_017029191.1:c.13398C>T
|
XP_016884680.1:p.His4466=
|
|
XM_017029192.1:c.13395C>T
|
XP_016884681.1:p.His4465=
|
|
XM_017029193.1:c.13377C>T
|
XP_016884682.1:p.His4459=
|
|
XM_017029194.1:c.13353C>T
|
XP_016884683.1:p.His4451=
|
|
XM_017029195.1:c.13350C>T
|
XP_016884684.1:p.His4450=
|
|
XM_017029196.1:c.13347C>T
|
XP_016884685.1:p.His4449=
|
|
XM_017029197.1:c.13299C>T
|
XP_016884686.1:p.His4433=
|
|
XM_017029198.2:c.13287C>T
|
XP_016884687.1:p.His4429=
|
|
XM_017029199.1:c.13287C>T
|
XP_016884688.1:p.His4429=
|
|
XM_017029200.1:c.13287C>T
|
XP_016884689.1:p.His4429=
|
|
XM_017029201.1:c.13287C>T
|
XP_016884690.1:p.His4429=
|
|
XM_017029202.1:c.13287C>T
|
XP_016884691.1:p.His4429=
|
|
XM_017029203.1:c.13287C>T
|
XP_016884692.1:p.His4429=
|
|
XM_017029204.1:c.13149C>T
|
XP_016884693.1:p.His4383=
|
|
XM_017029206.1:c.12996C>T
|
XP_016884695.1:p.His4332=
|
|
XM_024452322.1:c.13266C>T
|
XP_024308090.1:p.His4422=
|
|
NM_031407.7:c.13017C>T
MANE Select
|
NP_113584.3:p.His4339=
|
|