ENST00000357578.8:c.1303A=
MANE Select
|
ENSP00000350191.3:p.Thr435=
|
|
ENST00000479394.2:n.418A=
|
|
|
ENST00000672352.1:c.922A=
|
ENSP00000500876.1:p.Thr308=
|
|
ENST00000672652.1:c.1266A=
|
|
|
ENST00000348925.2:c.1342A=
|
ENSP00000314649.3:p.Thr448=
|
|
ENST00000357578.7:c.1303A=
|
ENSP00000350191.3:p.Thr435=
|
|
ENST00000479394.1:n.418A=
|
|
|
ENST00000491546.5:c.1219A=
|
ENSP00000417687.1:p.Thr407=
|
|
NM_001080.3:c.1303A=
MANE Select
|
NP_001071.1:p.Thr435=
|
|
NM_170740.1:c.1342A=
|
NP_733936.1:p.Thr448=
|
|
NM_001368954.1:c.1159A=
|
NP_001355883.1:p.Thr387=
|
|