ENST00000220616.9:c.8150T>G
MANE Select
|
ENSP00000220616.4:p.Phe2717Cys
|
|
ENST00000220616.8:c.8150T>G
|
ENSP00000220616.4:p.Phe2717Cys
|
|
ENST00000519178.5:c.3516T>G
|
|
|
ENST00000519543.5:c.2549T>G
|
ENSP00000430430.1:p.Phe850Cys
|
|
ENST00000521107.1:c.362T>G
|
ENSP00000430161.1:p.Phe121Cys
|
|
ENST00000522691.1:n.236T>G
|
|
|
ENST00000523756.5:c.4805T>G
|
|
|
NM_003235.4:c.8150T>G
|
NP_003226.4:p.Phe2717Cys
|
|
XM_005251038.3:c.7958T>G
|
XP_005251095.1:p.Phe2653Cys
|
|
XM_006716622.2:c.8087T>G
|
XP_006716685.1:p.Phe2696Cys
|
|
XM_005251038.4:c.7958T>G
|
XP_005251095.1:p.Phe2653Cys
|
|
XM_006716622.3:c.8087T>G
|
XP_006716685.1:p.Phe2696Cys
|
|
XM_017013793.1:c.8084T>G
|
XP_016869282.1:p.Phe2695Cys
|
|
XM_017013794.1:c.8015T>G
|
XP_016869283.1:p.Phe2672Cys
|
|
XM_017013795.1:c.7979T>G
|
XP_016869284.1:p.Phe2660Cys
|
|
XM_017013796.1:c.7931T>G
|
XP_016869285.1:p.Phe2644Cys
|
|
XM_017013797.1:c.7889T>G
|
XP_016869286.1:p.Phe2630Cys
|
|
NM_003235.5:c.8150T>G
MANE Select
|
NP_003226.4:p.Phe2717Cys
|
|