|
NM_005630.3:c.1660G>A
MANE Select
|
NP_005621.2:p.Gly554Arg
|
|
ENST00000310926.11:c.1660G>A
MANE Select
|
ENSP00000311291.4:p.Gly554Arg
|
|
NM_005630.2:c.1660G>A
|
NP_005621.2:p.Gly554Arg
|
|
ENST00000310926.8:c.1660G>A
|
ENSP00000311291.4:p.Gly554Arg
|
|
ENST00000481359.3:c.*222G>A
|
ENSP00000420028.3:n.*222G>A
|
|
ENST00000493729.5:c.1432G>A
|
ENSP00000418893.1:p.Gly478Arg
|
|
XM_011513090.1:c.1660G>A
|
XP_011511392.1:p.Gly554Arg
|
|
XM_017007077.1:c.1156G>A
|
XP_016862566.1:p.Gly386Arg
|
|
XM_024453721.1:c.1660G>A
|
XP_024309489.1:p.Gly554Arg
|