ENST00000265724.8:c.3069G>T
|
ENSP00000265724.3:p.Thr1023=
|
|
ENST00000622132.5:c.3069G>T
MANE Select
|
ENSP00000478255.1:p.Thr1023=
|
|
ENST00000265724.7:c.3069G>T
|
ENSP00000265724.3:p.Thr1023=
|
|
ENST00000475929.5:n.225G>T
|
|
|
ENST00000483831.1:n.627G>T
|
|
|
ENST00000488737.6:n.711G>T
|
|
|
ENST00000496821.5:n.697G>T
|
|
|
ENST00000543898.5:c.2877G>T
|
ENSP00000444095.1:p.Thr959=
|
|
ENST00000622132.4:c.3069G>T
|
ENSP00000478255.1:p.Thr1023=
|
|
NM_000927.4:c.3069G>T
|
NP_000918.2:p.Thr1023=
|
|
NM_001348944.1:c.3069G>T
|
NP_001335873.1:p.Thr1023=
|
|
NM_001348945.1:c.3279G>T
|
NP_001335874.1:p.Thr1093=
|
|
NM_001348946.1:c.3069G>T
|
NP_001335875.1:p.Thr1023=
|
|
NM_001348946.2:c.3069G>T
MANE Select
|
NP_001335875.1:p.Thr1023=
|
|
NM_000927.5:c.3069G>T
|
NP_000918.2:p.Thr1023=
|
|
NM_001348944.2:c.3069G>T
|
NP_001335873.1:p.Thr1023=
|
|
NM_001348945.2:c.3279G>T
|
NP_001335874.1:p.Thr1093=
|
|