|
NM_005957.5:c.1142G>A
MANE Select
|
NP_005948.3:p.Trp381Ter
|
|
ENST00000376590.9:c.1142G>A
MANE Select
|
ENSP00000365775.3:p.Trp381Ter
|
|
NM_001330358.1:c.1265G>A
|
NP_001317287.1:p.Trp422Ter
|
|
NM_001330358.2:c.1265G>A
|
NP_001317287.1:p.Trp422Ter
|
|
NM_005957.4:c.1142G>A , LRG_726t1:c.1142G>A
|
NP_005948.3:p.Trp381Ter
|
|
ENST00000376583.7:c.1265G>A
|
ENSP00000365767.3:p.Trp422Ter
|
|
ENST00000376585.5:c.1265G>A
|
ENSP00000365770.1:p.Trp422Ter
|
|
ENST00000376585.6:c.1265G>A
|
ENSP00000365770.1:p.Trp422Ter
|
|
ENST00000376590.7:c.1142G>A
|
ENSP00000365775.3:p.Trp381Ter
|
|
ENST00000376592.5:c.1142G>A
|
ENSP00000365777.1:p.Trp381Ter
|
|
ENST00000376592.6:c.1142G>A
|
ENSP00000365777.1:p.Trp381Ter
|
|
ENST00000423400.7:c.1262G>A
|
ENSP00000398908.3:p.Trp421Ter
|
|
ENST00000641407.1:c.1142G>A
|
ENSP00000493098.1:p.Trp381Ter
|
|
ENST00000641446.1:c.1142G>A
|
ENSP00000493262.1:p.Trp381Ter
|
|
ENST00000641747.1:c.*654G>A
|
ENSP00000493116.1:n.*654G>A
|
|
ENST00000641759.1:n.1511G>A
|
|
|
ENST00000641805.1:n.1659G>A
|
|
|
ENST00000641820.1:c.407G>A
|
ENSP00000492937.1:p.Trp136Ter
|
|
XM_005263458.2:c.1265G>A
|
XP_005263515.1:p.Trp422Ter
|
|
XM_005263460.3:c.1142G>A
|
XP_005263517.1:p.Trp381Ter
|
|
XM_005263460.5:c.1142G>A
|
XP_005263517.1:p.Trp381Ter
|
|
XM_005263461.3:c.1142G>A
|
XP_005263518.1:p.Trp381Ter
|
|
XM_005263462.3:c.1142G>A
|
XP_005263519.1:p.Trp381Ter
|
|
XM_005263462.4:c.1142G>A
|
XP_005263519.1:p.Trp381Ter
|
|
XM_005263463.2:c.896G>A
|
XP_005263520.1:p.Trp299Ter
|
|
XM_005263463.4:c.896G>A
|
XP_005263520.1:p.Trp299Ter
|
|
XM_011541495.1:c.1262G>A
|
XP_011539797.1:p.Trp421Ter
|
|
XM_011541495.3:c.1262G>A
|
XP_011539797.1:p.Trp421Ter
|
|
XM_011541496.1:c.1265G>A
|
XP_011539798.1:p.Trp422Ter
|
|
XM_011541496.3:c.1265G>A
|
XP_011539798.1:p.Trp422Ter
|
|
XM_017001328.2:c.1265G>A
|
XP_016856817.1:p.Trp422Ter
|
|
XM_024447198.1:c.896G>A
|
XP_024302966.1:p.Trp299Ter
|
|
XR_002956640.1:n.2243G>A
|
|
