ENST00000220616.9:c.8098T>G
MANE Select
|
ENSP00000220616.4:p.Phe2700Val
|
|
ENST00000220616.8:c.8098T>G
|
ENSP00000220616.4:p.Phe2700Val
|
|
ENST00000519178.5:c.3464T>G
|
|
|
ENST00000519543.5:c.2497T>G
|
ENSP00000430430.1:p.Phe833Val
|
|
ENST00000521107.1:c.310T>G
|
ENSP00000430161.1:p.Phe104Val
|
|
ENST00000522691.1:n.184T>G
|
|
|
ENST00000523756.5:c.4753T>G
|
|
|
NM_003235.4:c.8098T>G
|
NP_003226.4:p.Phe2700Val
|
|
XM_005251038.3:c.7906T>G
|
XP_005251095.1:p.Phe2636Val
|
|
XM_006716622.2:c.8035T>G
|
XP_006716685.1:p.Phe2679Val
|
|
XM_005251038.4:c.7906T>G
|
XP_005251095.1:p.Phe2636Val
|
|
XM_006716622.3:c.8035T>G
|
XP_006716685.1:p.Phe2679Val
|
|
XM_017013793.1:c.8032T>G
|
XP_016869282.1:p.Phe2678Val
|
|
XM_017013794.1:c.7963T>G
|
XP_016869283.1:p.Phe2655Val
|
|
XM_017013795.1:c.7927T>G
|
XP_016869284.1:p.Phe2643Val
|
|
XM_017013796.1:c.7879T>G
|
XP_016869285.1:p.Phe2627Val
|
|
XM_017013797.1:c.7837T>G
|
XP_016869286.1:p.Phe2613Val
|
|
NM_003235.5:c.8098T>G
MANE Select
|
NP_003226.4:p.Phe2700Val
|
|