ENST00000496887.7:c.980A>T
|
ENSP00000434560.2:p.Asp327Val
|
|
ENST00000646564.2:c.797A>T
|
ENSP00000495806.2:p.Asp266Val
|
|
ENST00000155840.12:c.1337A>T
MANE Select
|
ENSP00000155840.2:p.Asp446Val
|
|
ENST00000335475.6:c.956A>T
|
ENSP00000334497.5:p.Asp319Val
|
|
ENST00000646564.1:c.443A>T
|
ENSP00000495806.1:p.Asp148Val
|
|
ENST00000155840.9:c.1337A>T
|
ENSP00000155840.2:p.Asp446Val
|
|
ENST00000335475.5:c.956A>T
|
ENSP00000334497.5:p.Asp319Val
|
|
NM_000218.2:c.1337A>T , LRG_287t1:c.1337A>T
|
NP_000209.2:p.Asp446Val
|
|
NM_181798.1:c.956A>T , LRG_287t2:c.956A>T
|
NP_861463.1:p.Asp319Val
|
|
NM_000218.3:c.1337A>T
MANE Select
|
NP_000209.2:p.Asp446Val
|
|