|
NM_005630.3:c.763G>A
MANE Select
|
NP_005621.2:p.Gly255Arg
|
|
ENST00000310926.11:c.763G>A
MANE Select
|
ENSP00000311291.4:p.Gly255Arg
|
|
NM_005630.2:c.763G>A
|
NP_005621.2:p.Gly255Arg
|
|
ENST00000310926.8:c.763G>A
|
ENSP00000311291.4:p.Gly255Arg
|
|
ENST00000462770.5:n.521-2606G>A
|
|
|
ENST00000464676.5:n.1025G>A
|
|
|
ENST00000481359.3:c.763G>A
|
ENSP00000420028.3:p.Gly255Arg
|
|
ENST00000493729.5:c.535G>A
|
ENSP00000418893.1:p.Gly179Arg
|
|
XM_011513090.1:c.763G>A
|
XP_011511392.1:p.Gly255Arg
|
|
XM_017007077.1:c.259G>A
|
XP_016862566.1:p.Gly87Arg
|
|
XM_024453721.1:c.763G>A
|
XP_024309489.1:p.Gly255Arg
|