ENST00000369538.4:c.881G>C
|
ENSP00000358551.4:p.Arg294Thr
|
|
ENST00000520113.7:c.893G>C
MANE Select
|
ENSP00000430075.3:p.Arg298Thr
|
|
ENST00000637080.1:c.676G>C
|
ENSP00000489753.1:n.676G>C
|
|
ENST00000639077.1:n.558G>C
|
|
|
ENST00000369538.3:c.980G>C
|
ENSP00000358551.3:p.Arg327Thr
|
|
ENST00000520113.6:c.992G>C
|
ENSP00000430075.2:p.Arg331Thr
|
|
NM_000036.2:c.992G>C
|
NP_000027.2:p.Arg331Thr
|
|
NM_001172626.1:c.980G>C
|
NP_001166097.1:p.Arg327Thr
|
|
NM_000036.3:c.893G>C
MANE Select
|
NP_000027.3:p.Arg298Thr
|
|
NM_001172626.2:c.881G>C
|
NP_001166097.2:p.Arg294Thr
|
|