|
NM_021628.3:c.2065C>T
MANE Select
|
NP_067641.2:p.Arg689Trp
|
|
ENST00000448843.7:c.2065C>T
MANE Select
|
ENSP00000400581.2:p.Arg689Trp
|
|
NM_001165960.1:c.2461C>T
|
NP_001159432.1:p.Arg821Trp
|
|
NM_001369446.1:c.2062C>T
|
NP_001356375.1:p.Arg688Trp
|
|
NM_021628.2:c.2065C>T
|
NP_067641.2:p.Arg689Trp
|
|
ENST00000318227.3:c.2461C>T
|
ENSP00000314879.3:p.Arg821Trp
|
|
ENST00000318227.4:c.2065C>T
|
ENSP00000314879.4:p.Arg689Trp
|
|
ENST00000380149.5:c.2533C>T
|
ENSP00000369494.1:p.Arg845Trp
|
|
ENST00000380149.6:c.2065C>T
|
ENSP00000369494.2:p.Arg689Trp
|
|
ENST00000448843.6:c.2065C>T
|
ENSP00000400581.2:p.Arg689Trp
|
|
ENST00000583808.1:n.302C>T
|
|
|
XR_001752579.2:n.2216C>T
|
|
|
XR_001752580.2:n.2127C>T
|
|