ENST00000220616.9:c.8039C>G
MANE Select
|
ENSP00000220616.4:p.Thr2680Arg
|
|
ENST00000220616.8:c.8039C>G
|
ENSP00000220616.4:p.Thr2680Arg
|
|
ENST00000519178.5:c.3405C>G
|
|
|
ENST00000519543.5:c.2438C>G
|
ENSP00000430430.1:p.Thr813Arg
|
|
ENST00000521107.1:c.251C>G
|
ENSP00000430161.1:p.Thr84Arg
|
|
ENST00000522691.1:n.125C>G
|
|
|
ENST00000523756.5:c.4694C>G
|
|
|
NM_003235.4:c.8039C>G
|
NP_003226.4:p.Thr2680Arg
|
|
XM_005251038.3:c.7847C>G
|
XP_005251095.1:p.Thr2616Arg
|
|
XM_006716622.2:c.7976C>G
|
XP_006716685.1:p.Thr2659Arg
|
|
XM_005251038.4:c.7847C>G
|
XP_005251095.1:p.Thr2616Arg
|
|
XM_006716622.3:c.7976C>G
|
XP_006716685.1:p.Thr2659Arg
|
|
XM_017013793.1:c.7973C>G
|
XP_016869282.1:p.Thr2658Arg
|
|
XM_017013794.1:c.7904C>G
|
XP_016869283.1:p.Thr2635Arg
|
|
XM_017013795.1:c.7868C>G
|
XP_016869284.1:p.Thr2623Arg
|
|
XM_017013796.1:c.7820C>G
|
XP_016869285.1:p.Thr2607Arg
|
|
XM_017013797.1:c.7778C>G
|
XP_016869286.1:p.Thr2593Arg
|
|
NM_003235.5:c.8039C>G
MANE Select
|
NP_003226.4:p.Thr2680Arg
|
|