ENST00000296585.10:c.844A>T
MANE Select
|
ENSP00000296585.5:p.Thr282Ser
|
|
ENST00000296585.9:c.844A>T
|
ENSP00000296585.5:p.Thr282Ser
|
|
ENST00000503810.6:c.*188A>T
|
ENSP00000426489.1:n.*188A>T
|
|
ENST00000509814.5:c.844A>T
|
ENSP00000424397.1:p.Thr282Ser
|
|
ENST00000509960.5:c.844A>T
|
ENSP00000424642.1:p.Thr282Ser
|
|
ENST00000510722.1:c.844A>T
|
ENSP00000422145.1:p.Thr282Ser
|
|
ENST00000513685.5:c.*558A>T
|
ENSP00000422095.1:n.*558A>T
|
|
NM_002203.3:c.844A>T
|
NP_002194.2:p.Thr282Ser
|
|
NR_073103.1:n.987A>T
|
|
|
NR_073104.1:n.987A>T
|
|
|
NR_073105.1:n.987A>T
|
|
|
NR_073106.1:n.987A>T
|
|
|
NR_073107.1:n.866A>T
|
|
|
NM_002203.4:c.844A>T
MANE Select
|
NP_002194.2:p.Thr282Ser
|
|
NR_073103.2:n.961A>T
|
|
|
NR_073104.2:n.961A>T
|
|
|
NR_073105.2:n.961A>T
|
|
|
NR_073106.2:n.961A>T
|
|
|
NR_073107.2:n.840A>T
|
|
|