ENST00000296585.10:c.891T>C
MANE Select
|
ENSP00000296585.5:p.Asp297=
|
|
ENST00000296585.9:c.891T>C
|
ENSP00000296585.5:p.Asp297=
|
|
ENST00000503810.6:c.*235T>C
|
ENSP00000426489.1:n.*235T>C
|
|
ENST00000509814.5:c.891T>C
|
ENSP00000424397.1:p.Asp297=
|
|
ENST00000509960.5:c.891T>C
|
ENSP00000424642.1:p.Asp297=
|
|
ENST00000510722.1:c.891T>C
|
ENSP00000422145.1:p.Asp297=
|
|
ENST00000513685.5:c.*605T>C
|
ENSP00000422095.1:n.*605T>C
|
|
NM_002203.3:c.891T>C
|
NP_002194.2:p.Asp297=
|
|
NR_073103.1:n.1034T>C
|
|
|
NR_073104.1:n.1034T>C
|
|
|
NR_073105.1:n.1034T>C
|
|
|
NR_073106.1:n.1034T>C
|
|
|
NR_073107.1:n.913T>C
|
|
|
NM_002203.4:c.891T>C
MANE Select
|
NP_002194.2:p.Asp297=
|
|
NR_073103.2:n.1008T>C
|
|
|
NR_073104.2:n.1008T>C
|
|
|
NR_073105.2:n.1008T>C
|
|
|
NR_073106.2:n.1008T>C
|
|
|
NR_073107.2:n.887T>C
|
|
|