ENST00000525346.6:c.836T>C
|
ENSP00000435707.3:p.Ile279Thr
|
|
ENST00000526780.6:c.836T>C
|
ENSP00000435668.2:p.Ile279Thr
|
|
ENST00000527316.6:c.662T>C
|
ENSP00000435047.2:p.Ile221Thr
|
|
ENST00000682708.1:c.887T>C
|
ENSP00000506866.1:p.Ile296Thr
|
|
ENST00000682880.1:c.836T>C
|
ENSP00000507520.1:p.Ile279Thr
|
|
ENST00000683287.1:c.872T>C
|
ENSP00000507607.1:p.Ile291Thr
|
|
ENST00000683714.1:c.836T>C
|
ENSP00000508207.1:p.Ile279Thr
|
|
ENST00000684396.1:n.876T>C
|
|
|
ENST00000685320.1:c.251T>C
|
ENSP00000509319.1:p.Ile84Thr
|
|
ENST00000690257.1:c.740T>C
|
ENSP00000510750.1:p.Ile247Thr
|
|
ENST00000355527.8:c.836T>C
MANE Select
|
ENSP00000347717.4:p.Ile279Thr
|
|
ENST00000355527.7:c.836T>C
|
ENSP00000347717.3:p.Ile279Thr
|
|
ENST00000407721.6:c.836T>C
|
ENSP00000384739.2:p.Ile279Thr
|
|
ENST00000525137.1:c.203T>C
|
ENSP00000435956.1:p.Ile68Thr
|
|
ENST00000527316.5:c.740T>C
|
ENSP00000435047.1:p.Ile247Thr
|
|
ENST00000533800.5:c.86T>C
|
ENSP00000435011.1:p.Ile29Thr
|
|
ENST00000534795.5:c.192T>C
|
|
|
NM_001163817.1:c.836T>C
|
NP_001157289.1:p.Ile279Thr
|
|
NM_001360.2:c.836T>C , LRG_340t1:c.836T>C
|
NP_001351.2:p.Ile279Thr
|
|
XM_011544777.1:c.836T>C
|
XP_011543079.1:p.Ile279Thr
|
|
XM_011544777.2:c.836T>C
|
XP_011543079.1:p.Ile279Thr
|
|
NM_001163817.2:c.836T>C
|
NP_001157289.1:p.Ile279Thr
|
|
NM_001360.3:c.836T>C
MANE Select
|
NP_001351.2:p.Ile279Thr
|
|