ENST00000525346.6:c.1198T=
|
ENSP00000435707.3:p.Trp400=
|
|
ENST00000526780.6:c.1198T=
|
ENSP00000435668.2:p.Trp400=
|
|
ENST00000527316.6:c.1024T=
|
ENSP00000435047.2:p.Trp342=
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ENST00000682708.1:c.1249T=
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ENSP00000506866.1:p.Trp417=
|
|
ENST00000683287.1:c.1234T=
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ENSP00000507607.1:p.Trp412=
|
|
ENST00000683714.1:c.1206T=
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ENSP00000508207.1:p.Ser402=
|
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ENST00000684396.1:n.1238T=
|
|
|
ENST00000685320.1:c.613T=
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ENSP00000509319.1:p.Trp205=
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|
ENST00000690257.1:c.1102T=
|
ENSP00000510750.1:p.Trp368=
|
|
ENST00000355527.8:c.1198T=
MANE Select
|
ENSP00000347717.4:p.Trp400=
|
|
ENST00000355527.7:c.1198T=
|
ENSP00000347717.3:p.Trp400=
|
|
ENST00000407721.6:c.1198T=
|
ENSP00000384739.2:p.Trp400=
|
|
ENST00000525137.1:c.699T=
|
ENSP00000435956.1:p.Ser233=
|
|
ENST00000533800.5:c.448T=
|
ENSP00000435011.1:p.Trp150=
|
|
ENST00000534795.5:c.319+2207T=
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|
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NM_001163817.1:c.1198T=
|
NP_001157289.1:p.Trp400=
|
|
NM_001360.2:c.1198T= , LRG_340t1:c.1198T=
|
NP_001351.2:p.Trp400=
|
|
XM_011544777.1:c.1332T=
|
XP_011543079.1:p.Ser444=
|
|
XM_011544777.2:c.1332T=
|
XP_011543079.1:p.Ser444=
|
|
NM_001163817.2:c.1198T=
|
NP_001157289.1:p.Trp400=
|
|
NM_001360.3:c.1198T=
MANE Select
|
NP_001351.2:p.Trp400=
|
|