ENST00000269980.7:c.198A>C
MANE Select
|
ENSP00000269980.2:p.Glu66Asp
|
|
ENST00000269980.6:c.198A>C
|
ENSP00000269980.2:p.Glu66Asp
|
|
ENST00000457836.6:c.132A>C
|
ENSP00000416000.2:p.Glu44Asp
|
|
ENST00000538423.5:n.218A>C
|
|
|
ENST00000540732.3:c.300A>C
|
ENSP00000443246.1:p.Glu100Asp
|
|
ENST00000541315.1:c.5A>C
|
|
|
ENST00000542943.5:c.198A>C
|
ENSP00000440345.1:p.Glu66Asp
|
|
ENST00000595085.5:c.198A>C
|
ENSP00000471150.2:p.Glu66Asp
|
|
ENST00000604424.1:n.440A>C
|
|
|
NM_000709.3:c.198A>C
|
NP_000700.1:p.Glu66Asp
|
|
NM_001164783.1:c.198A>C
|
NP_001158255.1:p.Glu66Asp
|
|
NM_000709.4:c.198A>C
MANE Select
|
NP_000700.1:p.Glu66Asp
|
|
NM_001164783.2:c.198A>C
|
NP_001158255.1:p.Glu66Asp
|
|