ENST00000496887.7:c.702G>T
|
ENSP00000434560.2:p.Gln234His
|
|
ENST00000646564.2:c.519G>T
|
ENSP00000495806.2:p.Gln173His
|
|
ENST00000155840.12:c.963G>T
MANE Select
|
ENSP00000155840.2:p.Gln321His
|
|
ENST00000335475.6:c.582G>T
|
ENSP00000334497.5:p.Gln194His
|
|
ENST00000646564.1:c.165G>T
|
ENSP00000495806.1:p.Gln55His
|
|
ENST00000155840.9:c.963G>T
|
ENSP00000155840.2:p.Gln321His
|
|
ENST00000335475.5:c.582G>T
|
ENSP00000334497.5:p.Gln194His
|
|
NM_000218.2:c.963G>T , LRG_287t1:c.963G>T
|
NP_000209.2:p.Gln321His
|
|
NM_181798.1:c.582G>T , LRG_287t2:c.582G>T
|
NP_861463.1:p.Gln194His
|
|
NM_000218.3:c.963G>T
MANE Select
|
NP_000209.2:p.Gln321His
|
|