ENST00000347901.9:c.1332G>C
MANE Select
|
ENSP00000334002.4:p.Arg444Ser
|
|
ENST00000310778.5:c.1488G>C
|
ENSP00000309392.5:p.Arg496Ser
|
|
ENST00000341193.9:c.1281G>C
|
ENSP00000343170.5:p.Arg427Ser
|
|
ENST00000347901.8:c.1332G>C
|
ENSP00000334002.4:p.Arg444Ser
|
|
ENST00000393939.6:c.1257G>C
|
ENSP00000377513.2:p.Arg419Ser
|
|
NM_001079870.1:c.1281G>C
|
NP_001073339.1:p.Arg427Ser
|
|
NM_001079871.1:c.1257G>C
|
NP_001073340.1:p.Arg419Ser
|
|
NM_177977.2:c.1332G>C
|
NP_817084.2:p.Arg444Ser
|
|
NM_001367459.1:c.1428G>C
|
NP_001354388.1:p.Arg476Ser
|
|
NM_001367460.1:c.1392G>C
|
NP_001354389.1:p.Arg464Ser
|
|
NM_001367461.1:c.1257G>C
|
NP_001354390.1:p.Arg419Ser
|
|
NM_001367462.1:c.1257G>C
|
NP_001354391.1:p.Arg419Ser
|
|
NM_177977.3:c.1332G>C
MANE Select
|
NP_817084.2:p.Arg444Ser
|
|