ENST00000296585.10:c.915G>T
MANE Select
|
ENSP00000296585.5:p.Leu305=
|
|
ENST00000296585.9:c.915G>T
|
ENSP00000296585.5:p.Leu305=
|
|
ENST00000503810.6:c.*259G>T
|
ENSP00000426489.1:n.*259G>T
|
|
ENST00000509814.5:c.915G>T
|
ENSP00000424397.1:p.Leu305=
|
|
ENST00000509960.5:c.915G>T
|
ENSP00000424642.1:p.Leu305=
|
|
ENST00000510722.1:c.915G>T
|
ENSP00000422145.1:p.Leu305=
|
|
ENST00000513685.5:c.*629G>T
|
ENSP00000422095.1:n.*629G>T
|
|
NM_002203.3:c.915G>T
|
NP_002194.2:p.Leu305=
|
|
NR_073103.1:n.1058G>T
|
|
|
NR_073104.1:n.1058G>T
|
|
|
NR_073105.1:n.1058G>T
|
|
|
NR_073106.1:n.1058G>T
|
|
|
NR_073107.1:n.937G>T
|
|
|
NM_002203.4:c.915G>T
MANE Select
|
NP_002194.2:p.Leu305=
|
|
NR_073103.2:n.1032G>T
|
|
|
NR_073104.2:n.1032G>T
|
|
|
NR_073105.2:n.1032G>T
|
|
|
NR_073106.2:n.1032G>T
|
|
|
NR_073107.2:n.911G>T
|
|
|