ENST00000525346.6:c.1207G>A
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ENSP00000435707.3:p.Ala403Thr
|
|
ENST00000526780.6:c.1207G>A
|
ENSP00000435668.2:p.Ala403Thr
|
|
ENST00000527316.6:c.1033G>A
|
ENSP00000435047.2:p.Ala345Thr
|
|
ENST00000682708.1:c.1258G>A
|
ENSP00000506866.1:p.Ala420Thr
|
|
ENST00000683287.1:c.1243G>A
|
ENSP00000507607.1:p.Ala415Thr
|
|
ENST00000683714.1:c.1215G>A
|
ENSP00000508207.1:p.Trp405Ter
|
|
ENST00000684396.1:n.1247G>A
|
|
|
ENST00000685320.1:c.622G>A
|
ENSP00000509319.1:p.Ala208Thr
|
|
ENST00000690257.1:c.1111G>A
|
ENSP00000510750.1:p.Ala371Thr
|
|
ENST00000355527.8:c.1207G>A
MANE Select
|
ENSP00000347717.4:p.Ala403Thr
|
|
ENST00000355527.7:c.1207G>A
|
ENSP00000347717.3:p.Ala403Thr
|
|
ENST00000407721.6:c.1207G>A
|
ENSP00000384739.2:p.Ala403Thr
|
|
ENST00000525137.1:c.708G>A
|
ENSP00000435956.1:p.Trp236Ter
|
|
ENST00000533800.5:c.457G>A
|
ENSP00000435011.1:p.Ala153Thr
|
|
ENST00000534795.5:c.319+2216G>A
|
|
|
NM_001163817.1:c.1207G>A
|
NP_001157289.1:p.Ala403Thr
|
|
NM_001360.2:c.1207G>A , LRG_340t1:c.1207G>A
|
NP_001351.2:p.Ala403Thr
|
|
XM_011544777.1:c.1341G>A
|
XP_011543079.1:p.Trp447Ter
|
|
XM_011544777.2:c.1341G>A
|
XP_011543079.1:p.Trp447Ter
|
|
NM_001163817.2:c.1207G>A
|
NP_001157289.1:p.Ala403Thr
|
|
NM_001360.3:c.1207G>A
MANE Select
|
NP_001351.2:p.Ala403Thr
|
|