ENST00000357578.8:c.1224A>C
MANE Select
|
ENSP00000350191.3:p.Thr408=
|
|
ENST00000479394.2:n.339A>C
|
|
|
ENST00000672352.1:c.843A>C
|
ENSP00000500876.1:p.Thr281=
|
|
ENST00000672652.1:c.1187A>C
|
|
|
ENST00000348925.2:c.1263A>C
|
ENSP00000314649.3:p.Thr421=
|
|
ENST00000357578.7:c.1224A>C
|
ENSP00000350191.3:p.Thr408=
|
|
ENST00000479394.1:n.339A>C
|
|
|
ENST00000491546.5:c.1140A>C
|
ENSP00000417687.1:p.Thr380=
|
|
NM_001080.3:c.1224A>C
MANE Select
|
NP_001071.1:p.Thr408=
|
|
NM_170740.1:c.1263A>C
|
NP_733936.1:p.Thr421=
|
|
NM_001368954.1:c.1080A>C
|
NP_001355883.1:p.Thr360=
|
|