ENST00000220616.9:c.8170T>G
MANE Select
|
ENSP00000220616.4:p.Ser2724Ala
|
|
ENST00000220616.8:c.8170T>G
|
ENSP00000220616.4:p.Ser2724Ala
|
|
ENST00000519178.5:c.3536T>G
|
|
|
ENST00000519543.5:c.2569T>G
|
ENSP00000430430.1:p.Ser857Ala
|
|
ENST00000521107.1:c.382T>G
|
ENSP00000430161.1:p.Ser128Ala
|
|
ENST00000522691.1:n.256T>G
|
|
|
ENST00000523756.5:c.4825T>G
|
|
|
NM_003235.4:c.8170T>G
|
NP_003226.4:p.Ser2724Ala
|
|
XM_005251038.3:c.7978T>G
|
XP_005251095.1:p.Ser2660Ala
|
|
XM_006716622.2:c.8107T>G
|
XP_006716685.1:p.Ser2703Ala
|
|
XM_005251038.4:c.7978T>G
|
XP_005251095.1:p.Ser2660Ala
|
|
XM_006716622.3:c.8107T>G
|
XP_006716685.1:p.Ser2703Ala
|
|
XM_017013793.1:c.8104T>G
|
XP_016869282.1:p.Ser2702Ala
|
|
XM_017013794.1:c.8035T>G
|
XP_016869283.1:p.Ser2679Ala
|
|
XM_017013795.1:c.7999T>G
|
XP_016869284.1:p.Ser2667Ala
|
|
XM_017013796.1:c.7951T>G
|
XP_016869285.1:p.Ser2651Ala
|
|
XM_017013797.1:c.7909T>G
|
XP_016869286.1:p.Ser2637Ala
|
|
NM_003235.5:c.8170T>G
MANE Select
|
NP_003226.4:p.Ser2724Ala
|
|