ENST00000704099.1:c.12632G>C
|
ENSP00000515693.1:p.Arg4211Thr
|
|
ENST00000262854.11:c.12848G>C
MANE Select
|
ENSP00000262854.6:p.Arg4283Thr
|
|
ENST00000262854.10:c.12848G>C
|
ENSP00000262854.6:p.Arg4283Thr
|
|
ENST00000342160.7:c.12848G>C
|
ENSP00000340648.3:p.Arg4283Thr
|
|
ENST00000426907.5:c.3315G>C
|
|
|
ENST00000488459.1:n.161G>C
|
|
|
ENST00000612484.4:c.12821G>C
|
ENSP00000479451.1:p.Arg4274Thr
|
|
NM_031407.6:c.12848G>C
|
NP_113584.3:p.Arg4283Thr
|
|
XM_005261965.2:c.12848G>C
|
XP_005262022.1:p.Arg4283Thr
|
|
XM_011530746.1:c.13097G>C
|
XP_011529048.1:p.Arg4366Thr
|
|
XM_011530747.1:c.13097G>C
|
XP_011529049.1:p.Arg4366Thr
|
|
XM_011530748.1:c.13097G>C
|
XP_011529050.1:p.Arg4366Thr
|
|
XM_011530749.1:c.13097G>C
|
XP_011529051.1:p.Arg4366Thr
|
|
XM_011530750.1:c.13097G>C
|
XP_011529052.1:p.Arg4366Thr
|
|
XM_011530751.1:c.13097G>C
|
XP_011529053.1:p.Arg4366Thr
|
|
XM_011530752.1:c.13094G>C
|
XP_011529054.1:p.Arg4365Thr
|
|
XM_011530753.1:c.13052G>C
|
XP_011529055.1:p.Arg4351Thr
|
|
XM_011530754.1:c.13049G>C
|
XP_011529056.1:p.Arg4350Thr
|
|
XM_011530755.1:c.13046G>C
|
XP_011529057.1:p.Arg4349Thr
|
|
XM_011530756.1:c.12998G>C
|
XP_011529058.1:p.Arg4333Thr
|
|
XM_011530757.1:c.12695G>C
|
XP_011529059.1:p.Arg4232Thr
|
|
XM_005261965.4:c.12848G>C
|
XP_005262022.1:p.Arg4283Thr
|
|
XM_011530751.2:c.13097G>C
|
XP_011529053.1:p.Arg4366Thr
|
|
XM_017029191.1:c.13229G>C
|
XP_016884680.1:p.Arg4410Thr
|
|
XM_017029192.1:c.13226G>C
|
XP_016884681.1:p.Arg4409Thr
|
|
XM_017029193.1:c.13208G>C
|
XP_016884682.1:p.Arg4403Thr
|
|
XM_017029194.1:c.13184G>C
|
XP_016884683.1:p.Arg4395Thr
|
|
XM_017029195.1:c.13181G>C
|
XP_016884684.1:p.Arg4394Thr
|
|
XM_017029196.1:c.13178G>C
|
XP_016884685.1:p.Arg4393Thr
|
|
XM_017029197.1:c.13130G>C
|
XP_016884686.1:p.Arg4377Thr
|
|
XM_017029198.2:c.13118G>C
|
XP_016884687.1:p.Arg4373Thr
|
|
XM_017029199.1:c.13118G>C
|
XP_016884688.1:p.Arg4373Thr
|
|
XM_017029200.1:c.13118G>C
|
XP_016884689.1:p.Arg4373Thr
|
|
XM_017029201.1:c.13118G>C
|
XP_016884690.1:p.Arg4373Thr
|
|
XM_017029202.1:c.13118G>C
|
XP_016884691.1:p.Arg4373Thr
|
|
XM_017029203.1:c.13118G>C
|
XP_016884692.1:p.Arg4373Thr
|
|
XM_017029204.1:c.12980G>C
|
XP_016884693.1:p.Arg4327Thr
|
|
XM_017029206.1:c.12827G>C
|
XP_016884695.1:p.Arg4276Thr
|
|
XM_024452322.1:c.13097G>C
|
XP_024308090.1:p.Arg4366Thr
|
|
NM_031407.7:c.12848G>C
MANE Select
|
NP_113584.3:p.Arg4283Thr
|
|