|
NM_016023.5:c.343C>T
MANE Select
|
NP_057107.4:p.Arg115Ter
|
|
ENST00000404789.8:c.343C>T
MANE Select
|
ENSP00000384190.4:p.Arg115Ter
|
|
NM_001286745.1:c.40C>T
|
NP_001273674.1:p.Arg14Ter
|
|
NM_001286745.2:c.40C>T
|
NP_001273674.1:p.Arg14Ter
|
|
NM_001286745.3:c.40C>T
|
NP_001273674.1:p.Arg14Ter
|
|
NM_016023.3:c.433C>T
|
NP_057107.3:p.Arg145Ter
|
|
NM_016023.4:c.343C>T
|
NP_057107.4:p.Arg115Ter
|
|
ENST00000285420.8:c.433C>T
|
ENSP00000285420.4:p.Arg145Ter
|
|
ENST00000404789.7:c.343C>T
|
ENSP00000384190.4:p.Arg115Ter
|
|
ENST00000522894.5:c.*156C>T
|
ENSP00000428528.2:n.*156C>T
|
|
ENST00000524027.5:n.506C>T
|
|
|
ENST00000615618.1:c.40C>T
|
ENSP00000481196.1:p.Arg14Ter
|
|
ENST00000617869.4:c.433C>T
|
ENSP00000483706.1:p.Arg145Ter
|
|
XM_011517129.2:c.40C>T
|
XP_011515431.2:p.Arg14Ter
|