ENST00000357578.8:c.1257C>T
MANE Select
|
ENSP00000350191.3:p.Phe419=
|
|
ENST00000479394.2:n.372C>T
|
|
|
ENST00000672352.1:c.876C>T
|
ENSP00000500876.1:p.Phe292=
|
|
ENST00000672652.1:c.1220C>T
|
|
|
ENST00000348925.2:c.1296C>T
|
ENSP00000314649.3:p.Phe432=
|
|
ENST00000357578.7:c.1257C>T
|
ENSP00000350191.3:p.Phe419=
|
|
ENST00000479394.1:n.372C>T
|
|
|
ENST00000491546.5:c.1173C>T
|
ENSP00000417687.1:p.Phe391=
|
|
NM_001080.3:c.1257C>T
MANE Select
|
NP_001071.1:p.Phe419=
|
|
NM_170740.1:c.1296C>T
|
NP_733936.1:p.Phe432=
|
|
NM_001368954.1:c.1113C>T
|
NP_001355883.1:p.Phe371=
|
|