ENST00000357578.8:c.1321G=
MANE Select
|
ENSP00000350191.3:p.Gly441=
|
|
ENST00000479394.2:n.436G=
|
|
|
ENST00000672352.1:c.940G=
|
ENSP00000500876.1:p.Gly314=
|
|
ENST00000672652.1:c.1284G=
|
|
|
ENST00000348925.2:c.1360G=
|
ENSP00000314649.3:p.Gly454=
|
|
ENST00000357578.7:c.1321G=
|
ENSP00000350191.3:p.Gly441=
|
|
ENST00000479394.1:n.436G=
|
|
|
ENST00000491546.5:c.1237G=
|
ENSP00000417687.1:p.Gly413=
|
|
NM_001080.3:c.1321G=
MANE Select
|
NP_001071.1:p.Gly441=
|
|
NM_170740.1:c.1360G=
|
NP_733936.1:p.Gly454=
|
|
NM_001368954.1:c.1177G=
|
NP_001355883.1:p.Gly393=
|
|