ENST00000269980.7:c.652G>C
MANE Select
|
ENSP00000269980.2:p.Gly218Arg
|
|
ENST00000269980.6:c.652G>C
|
ENSP00000269980.2:p.Gly218Arg
|
|
ENST00000457836.6:c.586G>C
|
ENSP00000416000.2:p.Gly196Arg
|
|
ENST00000535632.5:n.281G>C
|
|
|
ENST00000538423.5:n.778G>C
|
|
|
ENST00000540732.3:c.754G>C
|
ENSP00000443246.1:p.Gly252Arg
|
|
ENST00000541315.1:c.552G>C
|
|
|
ENST00000542943.5:c.565G>C
|
ENSP00000440345.1:p.Gly189Arg
|
|
ENST00000545787.1:n.280G>C
|
|
|
ENST00000595085.5:c.652G>C
|
ENSP00000471150.2:p.Gly218Arg
|
|
NM_000709.3:c.652G>C
|
NP_000700.1:p.Gly218Arg
|
|
NM_001164783.1:c.652G>C
|
NP_001158255.1:p.Gly218Arg
|
|
NM_000709.4:c.652G>C
MANE Select
|
NP_000700.1:p.Gly218Arg
|
|
NM_001164783.2:c.652G>C
|
NP_001158255.1:p.Gly218Arg
|
|