ENST00000496887.7:c.1431A>C
|
ENSP00000434560.2:p.Glu477Asp
|
|
ENST00000646564.2:c.1248A>C
|
ENSP00000495806.2:p.Glu416Asp
|
|
ENST00000155840.12:c.1788A>C
MANE Select
|
ENSP00000155840.2:p.Glu596Asp
|
|
ENST00000335475.6:c.1407A>C
|
ENSP00000334497.5:p.Glu469Asp
|
|
ENST00000526095.2:c.192A>C
|
ENSP00000494939.1:p.Glu64Asp
|
|
ENST00000646564.1:c.894A>C
|
ENSP00000495806.1:p.Glu298Asp
|
|
ENST00000155840.9:c.1788A>C
|
ENSP00000155840.2:p.Glu596Asp
|
|
ENST00000335475.5:c.1407A>C
|
ENSP00000334497.5:p.Glu469Asp
|
|
ENST00000526095.1:n.295A>C
|
|
|
NM_000218.2:c.1788A>C , LRG_287t1:c.1788A>C
|
NP_000209.2:p.Glu596Asp
|
|
NM_181798.1:c.1407A>C , LRG_287t2:c.1407A>C
|
NP_861463.1:p.Glu469Asp
|
|
NM_000218.3:c.1788A>C
MANE Select
|
NP_000209.2:p.Glu596Asp
|
|