ENST00000220616.9:c.8161T>C
MANE Select
|
ENSP00000220616.4:p.Tyr2721His
|
|
ENST00000220616.8:c.8161T>C
|
ENSP00000220616.4:p.Tyr2721His
|
|
ENST00000519178.5:c.3527T>C
|
|
|
ENST00000519543.5:c.2560T>C
|
ENSP00000430430.1:p.Tyr854His
|
|
ENST00000521107.1:c.373T>C
|
ENSP00000430161.1:p.Tyr125His
|
|
ENST00000522691.1:n.247T>C
|
|
|
ENST00000523756.5:c.4816T>C
|
|
|
NM_003235.4:c.8161T>C
|
NP_003226.4:p.Tyr2721His
|
|
XM_005251038.3:c.7969T>C
|
XP_005251095.1:p.Tyr2657His
|
|
XM_006716622.2:c.8098T>C
|
XP_006716685.1:p.Tyr2700His
|
|
XM_005251038.4:c.7969T>C
|
XP_005251095.1:p.Tyr2657His
|
|
XM_006716622.3:c.8098T>C
|
XP_006716685.1:p.Tyr2700His
|
|
XM_017013793.1:c.8095T>C
|
XP_016869282.1:p.Tyr2699His
|
|
XM_017013794.1:c.8026T>C
|
XP_016869283.1:p.Tyr2676His
|
|
XM_017013795.1:c.7990T>C
|
XP_016869284.1:p.Tyr2664His
|
|
XM_017013796.1:c.7942T>C
|
XP_016869285.1:p.Tyr2648His
|
|
XM_017013797.1:c.7900T>C
|
XP_016869286.1:p.Tyr2634His
|
|
NM_003235.5:c.8161T>C
MANE Select
|
NP_003226.4:p.Tyr2721His
|
|