ENST00000496887.7:c.826T>C
|
ENSP00000434560.2:p.Tyr276His
|
|
ENST00000646564.2:c.643T>C
|
ENSP00000495806.2:p.Tyr215His
|
|
ENST00000155840.12:c.1183T>C
MANE Select
|
ENSP00000155840.2:p.Tyr395His
|
|
ENST00000335475.6:c.802T>C
|
ENSP00000334497.5:p.Tyr268His
|
|
ENST00000646564.1:c.289T>C
|
ENSP00000495806.1:p.Tyr97His
|
|
ENST00000155840.9:c.1183T>C
|
ENSP00000155840.2:p.Tyr395His
|
|
ENST00000335475.5:c.802T>C
|
ENSP00000334497.5:p.Tyr268His
|
|
NM_000218.2:c.1183T>C , LRG_287t1:c.1183T>C
|
NP_000209.2:p.Tyr395His
|
|
NM_181798.1:c.802T>C , LRG_287t2:c.802T>C
|
NP_861463.1:p.Tyr268His
|
|
NM_000218.3:c.1183T>C
MANE Select
|
NP_000209.2:p.Tyr395His
|
|