ENST00000585362.7:c.599G>A
|
ENSP00000473614.3:p.Trp200Ter
|
|
ENST00000593032.6:c.468G>A
|
ENSP00000465828.4:p.Val156=
|
|
ENST00000706713.1:c.482G>A
|
ENSP00000516510.1:p.Trp161Ter
|
|
ENST00000706714.1:c.468G>A
|
ENSP00000516511.1:p.Val156=
|
|
ENST00000706715.1:c.104G>A
|
ENSP00000516512.1:p.Trp35Ter
|
|
ENST00000354171.13:c.488G>A
MANE Select
|
ENSP00000346103.7:p.Trp163Ter
|
|
ENST00000589115.6:c.477-147G>A
|
ENSP00000466872.3:n.477-147G>A
|
|
ENST00000354171.12:c.488G>A
|
ENSP00000346103.7:p.Trp163Ter
|
|
ENST00000585480.1:c.221G>A
|
ENSP00000467900.1:p.Trp74Ter
|
|
ENST00000587648.5:c.368G>A
|
ENSP00000468349.1:p.Trp123Ter
|
|
ENST00000588919.5:c.407G>A
|
ENSP00000464989.3:p.Trp136Ter
|
|
ENST00000589115.5:c.477-147G>A
|
ENSP00000466872.2:n.477-147G>A
|
|
ENST00000592940.2:n.859G>A
|
|
|
ENST00000593032.5:c.468G>A
|
ENSP00000465828.3:p.Val156=
|
|
ENST00000611653.4:c.407G>A
|
ENSP00000483655.1:p.Trp136Ter
|
|
ENST00000616066.4:c.485G>A
|
ENSP00000485000.1:p.Trp162Ter
|
|
ENST00000622390.4:c.596G>A
|
ENSP00000477503.1:p.Trp199Ter
|
|
NM_001039847.2:c.488G>A
|
NP_001034936.1:p.Trp163Ter
|
|
NM_001039848.2:c.599G>A
|
NP_001034937.1:p.Trp200Ter
|
|
NM_002085.4:c.488G>A
|
NP_002076.2:p.Trp163Ter
|
|
NM_001039848.3:c.599G>A
|
NP_001034937.1:p.Trp200Ter
|
|
NM_001039847.3:c.488G>A
|
NP_001034936.1:p.Trp163Ter
|
|
NM_001039848.4:c.599G>A
|
NP_001034937.1:p.Trp200Ter
|
|
NM_001367832.1:c.407G>A
|
NP_001354761.1:p.Trp136Ter
|
|
NM_002085.5:c.488G>A
MANE Select
|
NP_002076.2:p.Trp163Ter
|
|