ENST00000496887.7:c.1249T>C
|
ENSP00000434560.2:p.Tyr417His
|
|
ENST00000646564.2:c.1066T>C
|
ENSP00000495806.2:p.Tyr356His
|
|
ENST00000155840.12:c.1606T>C
MANE Select
|
ENSP00000155840.2:p.Tyr536His
|
|
ENST00000335475.6:c.1225T>C
|
ENSP00000334497.5:p.Tyr409His
|
|
ENST00000646564.1:c.712T>C
|
ENSP00000495806.1:p.Tyr238His
|
|
ENST00000155840.9:c.1606T>C
|
ENSP00000155840.2:p.Tyr536His
|
|
ENST00000335475.5:c.1225T>C
|
ENSP00000334497.5:p.Tyr409His
|
|
NM_000218.2:c.1606T>C , LRG_287t1:c.1606T>C
|
NP_000209.2:p.Tyr536His
|
|
NM_181798.1:c.1225T>C , LRG_287t2:c.1225T>C
|
NP_861463.1:p.Tyr409His
|
|
NM_000218.3:c.1606T>C
MANE Select
|
NP_000209.2:p.Tyr536His
|
|