ENST00000496887.7:c.1250A>C
|
ENSP00000434560.2:p.Tyr417Ser
|
|
ENST00000646564.2:c.1067A>C
|
ENSP00000495806.2:p.Tyr356Ser
|
|
ENST00000155840.12:c.1607A>C
MANE Select
|
ENSP00000155840.2:p.Tyr536Ser
|
|
ENST00000335475.6:c.1226A>C
|
ENSP00000334497.5:p.Tyr409Ser
|
|
ENST00000646564.1:c.713A>C
|
ENSP00000495806.1:p.Tyr238Ser
|
|
ENST00000155840.9:c.1607A>C
|
ENSP00000155840.2:p.Tyr536Ser
|
|
ENST00000335475.5:c.1226A>C
|
ENSP00000334497.5:p.Tyr409Ser
|
|
NM_000218.2:c.1607A>C , LRG_287t1:c.1607A>C
|
NP_000209.2:p.Tyr536Ser
|
|
NM_181798.1:c.1226A>C , LRG_287t2:c.1226A>C
|
NP_861463.1:p.Tyr409Ser
|
|
NM_000218.3:c.1607A>C
MANE Select
|
NP_000209.2:p.Tyr536Ser
|
|