ENST00000322213.9:c.3253T>C
MANE Select
|
ENSP00000323421.3:p.Tyr1085His
|
|
ENST00000674590.1:c.2485T>C
|
ENSP00000502626.1:p.Tyr829His
|
|
ENST00000675504.1:c.3187T>C
|
ENSP00000502524.1:p.Tyr1063His
|
|
ENST00000322213.8:c.3253T>C
|
ENSP00000323421.3:p.Tyr1085His
|
|
ENST00000375340.10:c.3187T>C
|
ENSP00000364489.7:p.Tyr1063His
|
|
ENST00000469129.1:n.109T>C
|
|
|
ENST00000470241.2:c.543T>C
|
|
|
NM_001281463.1:c.3187T>C , LRG_773t1:c.3187T>C
|
NP_001268392.1:p.Tyr1063His
|
|
NM_006306.3:c.3253T>C , LRG_773t2:c.3253T>C
|
NP_006297.2:p.Tyr1085His
|
|
NM_006306.4:c.3253T>C
MANE Select
|
NP_006297.2:p.Tyr1085His
|
|