ENST00000355485.7:c.978G>T
MANE Select
|
ENSP00000347672.2:p.Arg326=
|
|
ENST00000310260.7:c.978G>T
|
ENSP00000310800.3:p.Arg326=
|
|
ENST00000355485.6:c.978G>T
|
ENSP00000347672.2:p.Arg326=
|
|
ENST00000369509.1:c.978G>T
|
ENSP00000358522.1:p.Arg326=
|
|
ENST00000369510.8:c.972G>T
|
ENSP00000358523.3:p.Arg324=
|
|
ENST00000474344.1:n.360G>T
|
|
|
ENST00000478369.5:n.262G>T
|
|
|
NM_001172411.1:c.972G>T
|
NP_001165882.1:p.Arg324=
|
|
NM_001172412.1:c.978G>T
|
NP_001165883.1:p.Arg326=
|
|
NM_138959.2:c.978G>T
|
NP_620409.1:p.Arg326=
|
|
NM_138959.3:c.978G>T
MANE Select
|
NP_620409.1:p.Arg326=
|
|
NM_001172411.2:c.972G>T
|
NP_001165882.1:p.Arg324=
|
|
NM_001172412.2:c.978G>T
|
NP_001165883.1:p.Arg326=
|
|