ENST00000220616.9:c.8089T>C
MANE Select
|
ENSP00000220616.4:p.Tyr2697His
|
|
ENST00000220616.8:c.8089T>C
|
ENSP00000220616.4:p.Tyr2697His
|
|
ENST00000519178.5:c.3455T>C
|
|
|
ENST00000519543.5:c.2488T>C
|
ENSP00000430430.1:p.Tyr830His
|
|
ENST00000521107.1:c.301T>C
|
ENSP00000430161.1:p.Tyr101His
|
|
ENST00000522691.1:n.175T>C
|
|
|
ENST00000523756.5:c.4744T>C
|
|
|
NM_003235.4:c.8089T>C
|
NP_003226.4:p.Tyr2697His
|
|
XM_005251038.3:c.7897T>C
|
XP_005251095.1:p.Tyr2633His
|
|
XM_006716622.2:c.8026T>C
|
XP_006716685.1:p.Tyr2676His
|
|
XM_005251038.4:c.7897T>C
|
XP_005251095.1:p.Tyr2633His
|
|
XM_006716622.3:c.8026T>C
|
XP_006716685.1:p.Tyr2676His
|
|
XM_017013793.1:c.8023T>C
|
XP_016869282.1:p.Tyr2675His
|
|
XM_017013794.1:c.7954T>C
|
XP_016869283.1:p.Tyr2652His
|
|
XM_017013795.1:c.7918T>C
|
XP_016869284.1:p.Tyr2640His
|
|
XM_017013796.1:c.7870T>C
|
XP_016869285.1:p.Tyr2624His
|
|
XM_017013797.1:c.7828T>C
|
XP_016869286.1:p.Tyr2610His
|
|
NM_003235.5:c.8089T>C
MANE Select
|
NP_003226.4:p.Tyr2697His
|
|