ENST00000220616.9:c.8045C>G
MANE Select
|
ENSP00000220616.4:p.Ala2682Gly
|
|
ENST00000220616.8:c.8045C>G
|
ENSP00000220616.4:p.Ala2682Gly
|
|
ENST00000519178.5:c.3411C>G
|
|
|
ENST00000519543.5:c.2444C>G
|
ENSP00000430430.1:p.Ala815Gly
|
|
ENST00000521107.1:c.257C>G
|
ENSP00000430161.1:p.Ala86Gly
|
|
ENST00000522691.1:n.131C>G
|
|
|
ENST00000523756.5:c.4700C>G
|
|
|
NM_003235.4:c.8045C>G
|
NP_003226.4:p.Ala2682Gly
|
|
XM_005251038.3:c.7853C>G
|
XP_005251095.1:p.Ala2618Gly
|
|
XM_006716622.2:c.7982C>G
|
XP_006716685.1:p.Ala2661Gly
|
|
XM_005251038.4:c.7853C>G
|
XP_005251095.1:p.Ala2618Gly
|
|
XM_006716622.3:c.7982C>G
|
XP_006716685.1:p.Ala2661Gly
|
|
XM_017013793.1:c.7979C>G
|
XP_016869282.1:p.Ala2660Gly
|
|
XM_017013794.1:c.7910C>G
|
XP_016869283.1:p.Ala2637Gly
|
|
XM_017013795.1:c.7874C>G
|
XP_016869284.1:p.Ala2625Gly
|
|
XM_017013796.1:c.7826C>G
|
XP_016869285.1:p.Ala2609Gly
|
|
XM_017013797.1:c.7784C>G
|
XP_016869286.1:p.Ala2595Gly
|
|
NM_003235.5:c.8045C>G
MANE Select
|
NP_003226.4:p.Ala2682Gly
|
|