ENST00000496887.7:c.1019A>T
|
ENSP00000434560.2:p.Asp340Val
|
|
ENST00000646564.2:c.836A>T
|
ENSP00000495806.2:p.Asp279Val
|
|
ENST00000155840.12:c.1376A>T
MANE Select
|
ENSP00000155840.2:p.Asp459Val
|
|
ENST00000335475.6:c.995A>T
|
ENSP00000334497.5:p.Asp332Val
|
|
ENST00000646564.1:c.482A>T
|
ENSP00000495806.1:p.Asp161Val
|
|
ENST00000155840.9:c.1376A>T
|
ENSP00000155840.2:p.Asp459Val
|
|
ENST00000335475.5:c.995A>T
|
ENSP00000334497.5:p.Asp332Val
|
|
NM_000218.2:c.1376A>T , LRG_287t1:c.1376A>T
|
NP_000209.2:p.Asp459Val
|
|
NM_181798.1:c.995A>T , LRG_287t2:c.995A>T
|
NP_861463.1:p.Asp332Val
|
|
NM_000218.3:c.1376A>T
MANE Select
|
NP_000209.2:p.Asp459Val
|
|