ENST00000296585.10:c.819T>G
MANE Select
|
ENSP00000296585.5:p.Ser273Arg
|
|
ENST00000296585.9:c.819T>G
|
ENSP00000296585.5:p.Ser273Arg
|
|
ENST00000503810.6:c.*163T>G
|
ENSP00000426489.1:n.*163T>G
|
|
ENST00000509814.5:c.819T>G
|
ENSP00000424397.1:p.Ser273Arg
|
|
ENST00000509960.5:c.819T>G
|
ENSP00000424642.1:p.Ser273Arg
|
|
ENST00000510722.1:c.819T>G
|
ENSP00000422145.1:p.Ser273Arg
|
|
ENST00000513685.5:c.*533T>G
|
ENSP00000422095.1:n.*533T>G
|
|
NM_002203.3:c.819T>G
|
NP_002194.2:p.Ser273Arg
|
|
NR_073103.1:n.962T>G
|
|
|
NR_073104.1:n.962T>G
|
|
|
NR_073105.1:n.962T>G
|
|
|
NR_073106.1:n.962T>G
|
|
|
NR_073107.1:n.841T>G
|
|
|
NM_002203.4:c.819T>G
MANE Select
|
NP_002194.2:p.Ser273Arg
|
|
NR_073103.2:n.936T>G
|
|
|
NR_073104.2:n.936T>G
|
|
|
NR_073105.2:n.936T>G
|
|
|
NR_073106.2:n.936T>G
|
|
|
NR_073107.2:n.815T>G
|
|
|