ENST00000704099.1:c.12669G>C
|
ENSP00000515693.1:p.Lys4223Asn
|
|
ENST00000262854.11:c.12885G>C
MANE Select
|
ENSP00000262854.6:p.Lys4295Asn
|
|
ENST00000262854.10:c.12885G>C
|
ENSP00000262854.6:p.Lys4295Asn
|
|
ENST00000342160.7:c.12885G>C
|
ENSP00000340648.3:p.Lys4295Asn
|
|
ENST00000426907.5:c.3352G>C
|
|
|
ENST00000488459.1:n.198G>C
|
|
|
ENST00000612484.4:c.12858G>C
|
ENSP00000479451.1:p.Lys4286Asn
|
|
NM_031407.6:c.12885G>C
|
NP_113584.3:p.Lys4295Asn
|
|
XM_005261965.2:c.12885G>C
|
XP_005262022.1:p.Lys4295Asn
|
|
XM_011530746.1:c.13134G>C
|
XP_011529048.1:p.Lys4378Asn
|
|
XM_011530747.1:c.13134G>C
|
XP_011529049.1:p.Lys4378Asn
|
|
XM_011530748.1:c.13134G>C
|
XP_011529050.1:p.Lys4378Asn
|
|
XM_011530749.1:c.13134G>C
|
XP_011529051.1:p.Lys4378Asn
|
|
XM_011530750.1:c.13134G>C
|
XP_011529052.1:p.Lys4378Asn
|
|
XM_011530751.1:c.13134G>C
|
XP_011529053.1:p.Lys4378Asn
|
|
XM_011530752.1:c.13131G>C
|
XP_011529054.1:p.Lys4377Asn
|
|
XM_011530753.1:c.13089G>C
|
XP_011529055.1:p.Lys4363Asn
|
|
XM_011530754.1:c.13086G>C
|
XP_011529056.1:p.Lys4362Asn
|
|
XM_011530755.1:c.13083G>C
|
XP_011529057.1:p.Lys4361Asn
|
|
XM_011530756.1:c.13035G>C
|
XP_011529058.1:p.Lys4345Asn
|
|
XM_011530757.1:c.12732G>C
|
XP_011529059.1:p.Lys4244Asn
|
|
XM_005261965.4:c.12885G>C
|
XP_005262022.1:p.Lys4295Asn
|
|
XM_011530751.2:c.13134G>C
|
XP_011529053.1:p.Lys4378Asn
|
|
XM_017029191.1:c.13266G>C
|
XP_016884680.1:p.Lys4422Asn
|
|
XM_017029192.1:c.13263G>C
|
XP_016884681.1:p.Lys4421Asn
|
|
XM_017029193.1:c.13245G>C
|
XP_016884682.1:p.Lys4415Asn
|
|
XM_017029194.1:c.13221G>C
|
XP_016884683.1:p.Lys4407Asn
|
|
XM_017029195.1:c.13218G>C
|
XP_016884684.1:p.Lys4406Asn
|
|
XM_017029196.1:c.13215G>C
|
XP_016884685.1:p.Lys4405Asn
|
|
XM_017029197.1:c.13167G>C
|
XP_016884686.1:p.Lys4389Asn
|
|
XM_017029198.2:c.13155G>C
|
XP_016884687.1:p.Lys4385Asn
|
|
XM_017029199.1:c.13155G>C
|
XP_016884688.1:p.Lys4385Asn
|
|
XM_017029200.1:c.13155G>C
|
XP_016884689.1:p.Lys4385Asn
|
|
XM_017029201.1:c.13155G>C
|
XP_016884690.1:p.Lys4385Asn
|
|
XM_017029202.1:c.13155G>C
|
XP_016884691.1:p.Lys4385Asn
|
|
XM_017029203.1:c.13155G>C
|
XP_016884692.1:p.Lys4385Asn
|
|
XM_017029204.1:c.13017G>C
|
XP_016884693.1:p.Lys4339Asn
|
|
XM_017029206.1:c.12864G>C
|
XP_016884695.1:p.Lys4288Asn
|
|
XM_024452322.1:c.13134G>C
|
XP_024308090.1:p.Lys4378Asn
|
|
NM_031407.7:c.12885G>C
MANE Select
|
NP_113584.3:p.Lys4295Asn
|
|