ENST00000369538.4:c.882G>T
|
ENSP00000358551.4:p.Arg294Ser
|
|
ENST00000520113.7:c.894G>T
MANE Select
|
ENSP00000430075.3:p.Arg298Ser
|
|
ENST00000637080.1:c.677G>T
|
ENSP00000489753.1:n.677G>T
|
|
ENST00000639077.1:n.559G>T
|
|
|
ENST00000369538.3:c.981G>T
|
ENSP00000358551.3:p.Arg327Ser
|
|
ENST00000520113.6:c.993G>T
|
ENSP00000430075.2:p.Arg331Ser
|
|
NM_000036.2:c.993G>T
|
NP_000027.2:p.Arg331Ser
|
|
NM_001172626.1:c.981G>T
|
NP_001166097.1:p.Arg327Ser
|
|
NM_000036.3:c.894G>T
MANE Select
|
NP_000027.3:p.Arg298Ser
|
|
NM_001172626.2:c.882G>T
|
NP_001166097.2:p.Arg294Ser
|
|