ENST00000220616.9:c.8063T>A
MANE Select
|
ENSP00000220616.4:p.Phe2688Tyr
|
|
ENST00000220616.8:c.8063T>A
|
ENSP00000220616.4:p.Phe2688Tyr
|
|
ENST00000519178.5:c.3429T>A
|
|
|
ENST00000519543.5:c.2462T>A
|
ENSP00000430430.1:p.Phe821Tyr
|
|
ENST00000521107.1:c.275T>A
|
ENSP00000430161.1:p.Phe92Tyr
|
|
ENST00000522691.1:n.149T>A
|
|
|
ENST00000523756.5:c.4718T>A
|
|
|
NM_003235.4:c.8063T>A
|
NP_003226.4:p.Phe2688Tyr
|
|
XM_005251038.3:c.7871T>A
|
XP_005251095.1:p.Phe2624Tyr
|
|
XM_006716622.2:c.8000T>A
|
XP_006716685.1:p.Phe2667Tyr
|
|
XM_005251038.4:c.7871T>A
|
XP_005251095.1:p.Phe2624Tyr
|
|
XM_006716622.3:c.8000T>A
|
XP_006716685.1:p.Phe2667Tyr
|
|
XM_017013793.1:c.7997T>A
|
XP_016869282.1:p.Phe2666Tyr
|
|
XM_017013794.1:c.7928T>A
|
XP_016869283.1:p.Phe2643Tyr
|
|
XM_017013795.1:c.7892T>A
|
XP_016869284.1:p.Phe2631Tyr
|
|
XM_017013796.1:c.7844T>A
|
XP_016869285.1:p.Phe2615Tyr
|
|
XM_017013797.1:c.7802T>A
|
XP_016869286.1:p.Phe2601Tyr
|
|
NM_003235.5:c.8063T>A
MANE Select
|
NP_003226.4:p.Phe2688Tyr
|
|