ENST00000229307.9:c.406T>C
MANE Select
|
ENSP00000229307.4:p.Tyr136His
|
|
ENST00000229307.8:c.406T>C
|
ENSP00000229307.4:p.Tyr136His
|
|
ENST00000526286.1:c.406T>C
|
ENSP00000435288.1:p.Tyr136His
|
|
ENST00000526434.2:n.550T>C
|
|
|
ENST00000541267.5:c.334T>C
|
ENSP00000444434.1:p.Tyr112His
|
|
NM_001297698.1:c.406T>C
|
NP_001284627.1:p.Tyr136His
|
|
NM_024865.3:c.406T>C
|
NP_079141.2:p.Tyr136His
|
|
XM_011520850.1:c.406T>C
|
XP_011519152.1:p.Tyr136His
|
|
XM_011520851.1:c.334T>C
|
XP_011519153.1:p.Tyr112His
|
|
XM_011520852.1:c.34T>C
|
XP_011519154.1:p.Tyr12His
|
|
NM_024865.4:c.406T>C
MANE Select
|
NP_079141.2:p.Tyr136His
|
|
NM_001297698.2:c.406T>C
|
NP_001284627.1:p.Tyr136His
|
|