ENST00000269980.7:c.1001G>A
MANE Select
|
ENSP00000269980.2:p.Gly334Glu
|
|
ENST00000269980.6:c.1001G>A
|
ENSP00000269980.2:p.Gly334Glu
|
|
ENST00000457836.6:c.1010G>A
|
ENSP00000416000.2:p.Gly337Glu
|
|
ENST00000540732.3:c.1103G>A
|
ENSP00000443246.1:p.Gly368Glu
|
|
ENST00000542943.5:c.914G>A
|
ENSP00000440345.1:p.Gly305Glu
|
|
ENST00000595085.5:c.922+306G>A
|
ENSP00000471150.2:n.922+306G>A
|
|
NM_000709.3:c.1001G>A
|
NP_000700.1:p.Gly334Glu
|
|
NM_001164783.1:c.998G>A
|
NP_001158255.1:p.Gly333Glu
|
|
NM_000709.4:c.1001G>A
MANE Select
|
NP_000700.1:p.Gly334Glu
|
|
NM_001164783.2:c.998G>A
|
NP_001158255.1:p.Gly333Glu
|
|