|
ENST00000301761.7:c.347G>A
MANE Select
|
ENSP00000301761.3:p.Trp116Ter
|
|
|
ENST00000301761.6:c.347G>A
|
ENSP00000301761.2:p.Trp116Ter
|
|
|
ENST00000359614.9:c.347G>A
|
ENSP00000352630.5:p.Trp116Ter
|
|
|
ENST00000534878.5:c.347G>A
|
ENSP00000471030.1:p.Trp116Ter
|
|
|
ENST00000536250.1:c.*349G>A
|
ENSP00000471120.1:n.*349G>A
|
|
|
ENST00000536670.5:n.373G>A
|
|
|
|
ENST00000537782.5:c.347G>A
|
ENSP00000469951.1:p.Trp116Ter
|
|
|
ENST00000538594.5:c.347G>A
|
ENSP00000440939.1:p.Trp116Ter
|
|
|
ENST00000541135.5:c.347G>A
|
ENSP00000443130.1:p.Trp116Ter
|
|
|
ENST00000542074.1:c.37-7851G>A
|
ENSP00000469670.1:n.37-7851G>A
|
|
|
ENST00000542794.5:c.*349G>A
|
ENSP00000439983.1:n.*349G>A
|
|
|
ENST00000543044.2:c.311G>A
|
ENSP00000440219.1:p.Trp104Ter
|
|
|
ENST00000543265.1:c.260+242G>A
|
ENSP00000443660.1:n.260+242G>A
|
|
|
ENST00000544025.5:n.442G>A
|
|
|
|
ENST00000544801.5:c.347G>A
|
ENSP00000442581.1:p.Trp116Ter
|
|
|
ENST00000544880.1:n.351G>A
|
|
|
|
NM_017841.2:c.347G>A , LRG_519t1:c.347G>A
|
NP_060311.1:p.Trp116Ter
|
|
|
NM_017841.4:c.347G>A
MANE Select
|
NP_060311.1:p.Trp116Ter
|
|
