ENST00000542639.6:c.504A>C
|
ENSP00000440846.1:p.Gly168=
|
|
ENST00000686683.1:c.213A>C
|
ENSP00000509063.1:p.Gly71=
|
|
ENST00000686980.1:n.1035A>C
|
|
|
ENST00000688006.1:c.504A>C
|
ENSP00000510311.1:p.Gly168=
|
|
ENST00000688859.1:n.459A>C
|
|
|
ENST00000689087.1:c.504A>C
|
ENSP00000508997.1:p.Gly168=
|
|
ENST00000693128.1:c.798A>C
|
ENSP00000508493.1:p.Gly266=
|
|
ENST00000338702.4:c.903A>C
MANE Select
|
ENSP00000340684.3:p.Gly301=
|
|
ENST00000338702.3:c.903A>C
|
ENSP00000340684.3:p.Gly301=
|
|
ENST00000542639.5:c.504A>C
|
ENSP00000440846.1:p.Gly168=
|
|
NM_000240.3:c.903A>C
|
NP_000231.1:p.Gly301=
|
|
NM_001270458.1:c.504A>C
|
NP_001257387.1:p.Gly168=
|
|
NM_000240.4:c.903A>C
MANE Select
|
NP_000231.1:p.Gly301=
|
|
NM_001270458.2:c.504A>C
|
NP_001257387.1:p.Gly168=
|
|