ENST00000322213.9:c.1531T>C
MANE Select
|
ENSP00000323421.3:p.Tyr511His
|
|
ENST00000674590.1:c.763T>C
|
ENSP00000502626.1:p.Tyr255His
|
|
ENST00000675065.1:n.883T>C
|
|
|
ENST00000675504.1:c.1465T>C
|
ENSP00000502524.1:p.Tyr489His
|
|
ENST00000322213.8:c.1531T>C
|
ENSP00000323421.3:p.Tyr511His
|
|
ENST00000375340.10:c.1465T>C
|
ENSP00000364489.7:p.Tyr489His
|
|
NM_001281463.1:c.1465T>C , LRG_773t1:c.1465T>C
|
NP_001268392.1:p.Tyr489His
|
|
NM_006306.3:c.1531T>C , LRG_773t2:c.1531T>C
|
NP_006297.2:p.Tyr511His
|
|
NM_006306.4:c.1531T>C
MANE Select
|
NP_006297.2:p.Tyr511His
|
|