ENST00000220616.9:c.8023T>A
MANE Select
|
ENSP00000220616.4:p.Ser2675Thr
|
|
ENST00000220616.8:c.8023T>A
|
ENSP00000220616.4:p.Ser2675Thr
|
|
ENST00000519178.5:c.3389T>A
|
|
|
ENST00000519543.5:c.2422T>A
|
ENSP00000430430.1:p.Ser808Thr
|
|
ENST00000521107.1:c.235T>A
|
ENSP00000430161.1:p.Ser79Thr
|
|
ENST00000522691.1:n.109T>A
|
|
|
ENST00000523756.5:c.4678T>A
|
|
|
NM_003235.4:c.8023T>A
|
NP_003226.4:p.Ser2675Thr
|
|
XM_005251038.3:c.7831T>A
|
XP_005251095.1:p.Ser2611Thr
|
|
XM_006716622.2:c.7960T>A
|
XP_006716685.1:p.Ser2654Thr
|
|
XM_005251038.4:c.7831T>A
|
XP_005251095.1:p.Ser2611Thr
|
|
XM_006716622.3:c.7960T>A
|
XP_006716685.1:p.Ser2654Thr
|
|
XM_017013793.1:c.7957T>A
|
XP_016869282.1:p.Ser2653Thr
|
|
XM_017013794.1:c.7888T>A
|
XP_016869283.1:p.Ser2630Thr
|
|
XM_017013795.1:c.7852T>A
|
XP_016869284.1:p.Ser2618Thr
|
|
XM_017013796.1:c.7804T>A
|
XP_016869285.1:p.Ser2602Thr
|
|
XM_017013797.1:c.7762T>A
|
XP_016869286.1:p.Ser2588Thr
|
|
NM_003235.5:c.8023T>A
MANE Select
|
NP_003226.4:p.Ser2675Thr
|
|