|
ENST00000411732.4:c.1075C>T
|
ENSP00000387634.1:p.Arg359Trp
|
|
|
ENST00000439032.6:c.1765C>T
|
ENSP00000509775.1:n.1765C>T
|
|
|
ENST00000637191.2:c.1225C>T
|
ENSP00000490154.2:p.Arg409Trp
|
|
|
ENST00000690143.1:c.*1157C>T
|
ENSP00000510306.1:n.*1157C>T
|
|
|
ENST00000691610.1:c.1264C>T
|
ENSP00000509830.1:p.Arg422Trp
|
|
|
ENST00000242480.4:c.1225C>T
MANE Select
|
ENSP00000242480.3:p.Arg409Trp
|
|
|
ENST00000411732.3:c.1075C>T
|
ENSP00000387634.1:p.Arg359Trp
|
|
|
ENST00000639815.1:n.109-451C>T
|
|
|
|
ENST00000242480.3:c.1225C>T
|
ENSP00000242480.3:p.Arg409Trp
|
|
|
ENST00000411732.2:c.1075C>T
|
ENSP00000387634.1:p.Arg359Trp
|
|
|
ENST00000439032.4:c.1225C>T
|
ENSP00000402040.1:p.Arg409Trp
|
|
|
NM_000399.3:c.1225C>T , LRG_239t1:c.1225C>T
|
NP_000390.2:p.Arg409Trp
|
|
|
NM_001136177.1:c.1225C>T
|
NP_001129649.1:p.Arg409Trp
|
|
|
NM_001136178.1:c.1225C>T
|
NP_001129650.1:p.Arg409Trp
|
|
|
NM_001136179.1:c.1075C>T
|
NP_001129651.1:p.Arg359Trp
|
|
|
XM_011539427.1:c.1264C>T
|
XP_011537729.1:p.Arg422Trp
|
|
|
XM_011539428.1:c.1075C>T
|
XP_011537730.1:p.Arg359Trp
|
|
|
XM_011539429.1:c.1075C>T
|
XP_011537731.1:p.Arg359Trp
|
|
|
NM_000399.4:c.1225C>T
|
NP_000390.2:p.Arg409Trp
|
|
|
NM_001136177.2:c.1225C>T
|
NP_001129649.1:p.Arg409Trp
|
|
|
NM_001136179.2:c.1075C>T
|
NP_001129651.1:p.Arg359Trp
|
|
|
NM_001321037.1:c.1075C>T
|
NP_001307966.1:p.Arg359Trp
|
|
|
NM_000399.5:c.1225C>T
MANE Select
|
NP_000390.2:p.Arg409Trp
|
|
|
NM_001136177.3:c.1225C>T
|
NP_001129649.1:p.Arg409Trp
|
|
|
NM_001136179.3:c.1075C>T
|
NP_001129651.1:p.Arg359Trp
|
|
|
NM_001321037.2:c.1075C>T
|
NP_001307966.1:p.Arg359Trp
|
|
|
NM_001136178.2:c.1225C>T
|
NP_001129650.1:p.Arg409Trp
|
|
