|
ENST00000627394.3:c.1005G>A
|
ENSP00000485925.2:p.Trp335Ter
|
|
|
ENST00000683929.1:c.1005G>A
|
ENSP00000507689.1:p.Trp335Ter
|
|
|
ENST00000684632.1:n.1384G>A
|
|
|
|
ENST00000566780.6:c.1005G>A
MANE Select
|
ENSP00000457230.1:p.Trp335Ter
|
|
|
ENST00000402655.6:c.409+317547G>A
|
ENSP00000384238.2:n.409+317547G>A
|
|
|
ENST00000406884.6:c.516+268412G>A
|
ENSP00000384495.2:n.516+268412G>A
|
|
|
ENST00000408984.7:c.1005G>A
|
ENSP00000386161.3:p.Trp335Ter
|
|
|
ENST00000539474.6:c.409+317547G>A
|
ENSP00000445210.2:n.409+317547G>A
|
|
|
ENST00000566780.5:c.1005G>A
|
ENSP00000457230.1:p.Trp335Ter
|
|
|
ENST00000569332.5:c.*802G>A
|
ENSP00000454788.1:n.*802G>A
|
|
|
ENST00000620008.1:c.399G>A
|
ENSP00000482648.1:p.Trp133Ter
|
|
|
NM_001291997.1:c.666G>A
|
NP_001278926.1:p.Trp222Ter
|
|
|
NM_016373.3:c.1005G>A
|
NP_057457.1:p.Trp335Ter
|
|
|
XM_006721195.2:c.1005G>A
|
XP_006721258.1:p.Trp335Ter
|
|
|
XM_011523100.1:c.1005G>A
|
XP_011521402.1:p.Trp335Ter
|
|
|
XM_011523101.1:c.1005G>A
|
XP_011521403.1:p.Trp335Ter
|
|
|
XM_011523102.1:c.1005G>A
|
XP_011521404.1:p.Trp335Ter
|
|
|
XM_011523103.1:c.1005G>A
|
XP_011521405.1:p.Trp335Ter
|
|
|
XM_011523104.1:c.1005G>A
|
XP_011521406.1:p.Trp335Ter
|
|
|
XR_933765.1:n.3418+1619C>T
|
|
|
|
XM_011523101.3:c.1005G>A
|
XP_011521403.1:p.Trp335Ter
|
|
|
XM_011523103.3:c.1005G>A
|
XP_011521405.1:p.Trp335Ter
|
|
|
XM_011523104.3:c.1005G>A
|
XP_011521406.1:p.Trp335Ter
|
|
|
NM_016373.4:c.1005G>A
MANE Select
|
NP_057457.1:p.Trp335Ter
|
|
|
NM_001291997.2:c.666G>A
|
NP_001278926.1:p.Trp222Ter
|
|
