ENST00000269980.7:c.1194G>C
MANE Select
|
ENSP00000269980.2:p.Glu398Asp
|
|
ENST00000269980.6:c.1194G>C
|
ENSP00000269980.2:p.Glu398Asp
|
|
ENST00000457836.6:c.1203G>C
|
ENSP00000416000.2:p.Glu401Asp
|
|
ENST00000540732.3:c.1296G>C
|
ENSP00000443246.1:p.Glu432Asp
|
|
ENST00000544905.1:c.62-38G>C
|
|
|
ENST00000595085.5:c.922+1767G>C
|
ENSP00000471150.2:n.922+1767G>C
|
|
NM_000709.3:c.1194G>C
|
NP_000700.1:p.Glu398Asp
|
|
NM_001164783.1:c.1191G>C
|
NP_001158255.1:p.Glu397Asp
|
|
NM_000709.4:c.1194G>C
MANE Select
|
NP_000700.1:p.Glu398Asp
|
|
NM_001164783.2:c.1191G>C
|
NP_001158255.1:p.Glu397Asp
|
|