ENST00000450565.8:c.277C>T
MANE Select
|
ENSP00000411658.3:p.Arg93Cys
|
|
ENST00000269200.5:n.275C>T
|
|
|
ENST00000450565.7:c.277C>T
|
ENSP00000411658.3:p.Arg93Cys
|
|
ENST00000579794.1:c.277C>T
|
ENSP00000462647.1:p.Arg93Cys
|
|
ENST00000581602.1:n.268C>T
|
|
|
NM_001099733.1:c.277C>T
|
NP_001093203.1:p.Arg93Cys
|
|
NM_001117.4:c.277C>T
|
NP_001108.2:p.Arg93Cys
|
|
XM_005258081.2:c.760C>T
|
XP_005258138.1:p.Arg254Cys
|
|
XM_005258081.4:c.694C>T
|
XP_005258138.2:p.Arg232Cys
|
|
NM_001099733.2:c.277C>T
MANE Select
|
NP_001093203.1:p.Arg93Cys
|
|
NM_001117.5:c.277C>T
|
NP_001108.2:p.Arg93Cys
|
|