ENST00000369538.4:c.1081G>A
|
ENSP00000358551.4:p.Gly361Arg
|
|
ENST00000520113.7:c.1093G>A
MANE Select
|
ENSP00000430075.3:p.Gly365Arg
|
|
ENST00000637080.1:c.876G>A
|
ENSP00000489753.1:n.876G>A
|
|
ENST00000639077.1:n.758G>A
|
|
|
ENST00000369538.3:c.1180G>A
|
ENSP00000358551.3:p.Gly394Arg
|
|
ENST00000520113.6:c.1192G>A
|
ENSP00000430075.2:p.Gly398Arg
|
|
NM_000036.2:c.1192G>A
|
NP_000027.2:p.Gly398Arg
|
|
NM_001172626.1:c.1180G>A
|
NP_001166097.1:p.Gly394Arg
|
|
NM_000036.3:c.1093G>A
MANE Select
|
NP_000027.3:p.Gly365Arg
|
|
NM_001172626.2:c.1081G>A
|
NP_001166097.2:p.Gly361Arg
|
|