ENST00000525346.6:c.1213C>T
|
ENSP00000435707.3:p.His405Tyr
|
|
ENST00000526780.6:c.1213C>T
|
ENSP00000435668.2:p.His405Tyr
|
|
ENST00000527316.6:c.1039C>T
|
ENSP00000435047.2:p.His347Tyr
|
|
ENST00000682708.1:c.1264C>T
|
ENSP00000506866.1:p.His422Tyr
|
|
ENST00000683287.1:c.1249C>T
|
ENSP00000507607.1:p.His417Tyr
|
|
ENST00000683714.1:c.1221C>T
|
ENSP00000508207.1:p.Ala407=
|
|
ENST00000684396.1:n.1253C>T
|
|
|
ENST00000685320.1:c.628C>T
|
ENSP00000509319.1:p.His210Tyr
|
|
ENST00000690257.1:c.1117C>T
|
ENSP00000510750.1:p.His373Tyr
|
|
ENST00000355527.8:c.1213C>T
MANE Select
|
ENSP00000347717.4:p.His405Tyr
|
|
ENST00000355527.7:c.1213C>T
|
ENSP00000347717.3:p.His405Tyr
|
|
ENST00000407721.6:c.1213C>T
|
ENSP00000384739.2:p.His405Tyr
|
|
ENST00000525137.1:c.714C>T
|
ENSP00000435956.1:p.Ala238=
|
|
ENST00000533800.5:c.463C>T
|
ENSP00000435011.1:p.His155Tyr
|
|
ENST00000534795.5:c.319+2222C>T
|
|
|
NM_001163817.1:c.1213C>T
|
NP_001157289.1:p.His405Tyr
|
|
NM_001360.2:c.1213C>T , LRG_340t1:c.1213C>T
|
NP_001351.2:p.His405Tyr
|
|
XM_011544777.1:c.1347C>T
|
XP_011543079.1:p.Ala449=
|
|
XM_011544777.2:c.1347C>T
|
XP_011543079.1:p.Ala449=
|
|
NM_001163817.2:c.1213C>T
|
NP_001157289.1:p.His405Tyr
|
|
NM_001360.3:c.1213C>T
MANE Select
|
NP_001351.2:p.His405Tyr
|
|