ENST00000269980.7:c.979G>C
MANE Select
|
ENSP00000269980.2:p.Glu327Gln
|
|
ENST00000269980.6:c.979G>C
|
ENSP00000269980.2:p.Glu327Gln
|
|
ENST00000457836.6:c.913G>C
|
ENSP00000416000.2:p.Glu305Gln
|
|
ENST00000535632.5:n.608G>C
|
|
|
ENST00000540732.3:c.1081G>C
|
ENSP00000443246.1:p.Glu361Gln
|
|
ENST00000542943.5:c.892G>C
|
ENSP00000440345.1:p.Glu298Gln
|
|
ENST00000595085.5:c.922+57G>C
|
ENSP00000471150.2:n.922+57G>C
|
|
NM_000709.3:c.979G>C
|
NP_000700.1:p.Glu327Gln
|
|
NM_001164783.1:c.976G>C
|
NP_001158255.1:p.Glu326Gln
|
|
NM_000709.4:c.979G>C
MANE Select
|
NP_000700.1:p.Glu327Gln
|
|
NM_001164783.2:c.976G>C
|
NP_001158255.1:p.Glu326Gln
|
|