ENST00000525346.6:c.1046A>T
|
ENSP00000435707.3:p.Tyr349Phe
|
|
ENST00000526780.6:c.1046A>T
|
ENSP00000435668.2:p.Tyr349Phe
|
|
ENST00000527316.6:c.872A>T
|
ENSP00000435047.2:p.Tyr291Phe
|
|
ENST00000682708.1:c.1097A>T
|
ENSP00000506866.1:p.Tyr366Phe
|
|
ENST00000683287.1:c.1082A>T
|
ENSP00000507607.1:p.Tyr361Phe
|
|
ENST00000683714.1:c.1054A>T
|
ENSP00000508207.1:p.Thr352Ser
|
|
ENST00000684396.1:n.1086A>T
|
|
|
ENST00000685320.1:c.461A>T
|
ENSP00000509319.1:p.Tyr154Phe
|
|
ENST00000690257.1:c.950A>T
|
ENSP00000510750.1:p.Tyr317Phe
|
|
ENST00000355527.8:c.1046A>T
MANE Select
|
ENSP00000347717.4:p.Tyr349Phe
|
|
ENST00000355527.7:c.1046A>T
|
ENSP00000347717.3:p.Tyr349Phe
|
|
ENST00000407721.6:c.1046A>T
|
ENSP00000384739.2:p.Tyr349Phe
|
|
ENST00000525137.1:c.547A>T
|
ENSP00000435956.1:p.Thr183Ser
|
|
ENST00000533800.5:c.296A>T
|
ENSP00000435011.1:p.Tyr99Phe
|
|
ENST00000534795.5:c.319+2055A>T
|
|
|
NM_001163817.1:c.1046A>T
|
NP_001157289.1:p.Tyr349Phe
|
|
NM_001360.2:c.1046A>T , LRG_340t1:c.1046A>T
|
NP_001351.2:p.Tyr349Phe
|
|
XM_011544777.1:c.1180A>T
|
XP_011543079.1:p.Thr394Ser
|
|
XM_011544777.2:c.1180A>T
|
XP_011543079.1:p.Thr394Ser
|
|
NM_001163817.2:c.1046A>T
|
NP_001157289.1:p.Tyr349Phe
|
|
NM_001360.3:c.1046A>T
MANE Select
|
NP_001351.2:p.Tyr349Phe
|
|