ENST00000525346.6:c.1232A>T
|
ENSP00000435707.3:p.Asp411Val
|
|
ENST00000526780.6:c.1232A>T
|
ENSP00000435668.2:p.Asp411Val
|
|
ENST00000527316.6:c.1058A>T
|
ENSP00000435047.2:p.Asp353Val
|
|
ENST00000682708.1:c.1283A>T
|
ENSP00000506866.1:p.Asp428Val
|
|
ENST00000683287.1:c.1268A>T
|
ENSP00000507607.1:p.Asp423Val
|
|
ENST00000683714.1:c.1240A>T
|
ENSP00000508207.1:p.Thr414Ser
|
|
ENST00000684396.1:n.1272A>T
|
|
|
ENST00000685320.1:c.647A>T
|
ENSP00000509319.1:p.Asp216Val
|
|
ENST00000690257.1:c.1136A>T
|
ENSP00000510750.1:p.Asp379Val
|
|
ENST00000355527.8:c.1232A>T
MANE Select
|
ENSP00000347717.4:p.Asp411Val
|
|
ENST00000355527.7:c.1232A>T
|
ENSP00000347717.3:p.Asp411Val
|
|
ENST00000407721.6:c.1232A>T
|
ENSP00000384739.2:p.Asp411Val
|
|
ENST00000525137.1:c.733A>T
|
ENSP00000435956.1:p.Thr245Ser
|
|
ENST00000533800.5:c.482A>T
|
ENSP00000435011.1:p.Asp161Val
|
|
ENST00000534795.5:c.319+2241A>T
|
|
|
NM_001163817.1:c.1232A>T
|
NP_001157289.1:p.Asp411Val
|
|
NM_001360.2:c.1232A>T , LRG_340t1:c.1232A>T
|
NP_001351.2:p.Asp411Val
|
|
XM_011544777.1:c.1366A>T
|
XP_011543079.1:p.Thr456Ser
|
|
XM_011544777.2:c.1366A>T
|
XP_011543079.1:p.Thr456Ser
|
|
NM_001163817.2:c.1232A>T
|
NP_001157289.1:p.Asp411Val
|
|
NM_001360.3:c.1232A>T
MANE Select
|
NP_001351.2:p.Asp411Val
|
|