ENST00000369538.4:c.1142G>C
|
ENSP00000358551.4:p.Ser381Thr
|
|
ENST00000520113.7:c.1154G>C
MANE Select
|
ENSP00000430075.3:p.Ser385Thr
|
|
ENST00000637080.1:c.937G>C
|
ENSP00000489753.1:n.937G>C
|
|
ENST00000639077.1:n.819G>C
|
|
|
ENST00000369538.3:c.1241G>C
|
ENSP00000358551.3:p.Ser414Thr
|
|
ENST00000520113.6:c.1253G>C
|
ENSP00000430075.2:p.Ser418Thr
|
|
NM_000036.2:c.1253G>C
|
NP_000027.2:p.Ser418Thr
|
|
NM_001172626.1:c.1241G>C
|
NP_001166097.1:p.Ser414Thr
|
|
NM_000036.3:c.1154G>C
MANE Select
|
NP_000027.3:p.Ser385Thr
|
|
NM_001172626.2:c.1142G>C
|
NP_001166097.2:p.Ser381Thr
|
|