ENST00000525346.6:c.1390G>A
|
ENSP00000435707.3:p.Ala464Thr
|
|
ENST00000526780.6:c.1390G>A
|
ENSP00000435668.2:p.Ala464Thr
|
|
ENST00000527316.6:c.1216G>A
|
ENSP00000435047.2:p.Ala406Thr
|
|
ENST00000682708.1:c.1441G>A
|
ENSP00000506866.1:p.Ala481Thr
|
|
ENST00000683287.1:c.1426G>A
|
ENSP00000507607.1:p.Ala476Thr
|
|
ENST00000683714.1:c.*153G>A
|
ENSP00000508207.1:n.*153G>A
|
|
ENST00000684396.1:n.1430G>A
|
|
|
ENST00000685320.1:c.805G>A
|
ENSP00000509319.1:p.Ala269Thr
|
|
ENST00000690257.1:c.1294G>A
|
ENSP00000510750.1:p.Ala432Thr
|
|
ENST00000355527.8:c.1390G>A
MANE Select
|
ENSP00000347717.4:p.Ala464Thr
|
|
ENST00000355527.7:c.1390G>A
|
ENSP00000347717.3:p.Ala464Thr
|
|
ENST00000407721.6:c.1390G>A
|
ENSP00000384739.2:p.Ala464Thr
|
|
ENST00000525137.1:c.891G>A
|
ENSP00000435956.1:n.891G>A
|
|
ENST00000533800.5:c.611+29G>A
|
ENSP00000435011.1:n.611+29G>A
|
|
ENST00000534795.5:c.319+2399G>A
|
|
|
NM_001163817.1:c.1390G>A
|
NP_001157289.1:p.Ala464Thr
|
|
NM_001360.2:c.1390G>A , LRG_340t1:c.1390G>A
|
NP_001351.2:p.Ala464Thr
|
|
XM_011544777.1:c.*153G>A
|
XP_011543079.1:n.*153G>A
|
|
XM_011544777.2:c.*153G>A
|
XP_011543079.1:n.*153G>A
|
|
NM_001163817.2:c.1390G>A
|
NP_001157289.1:p.Ala464Thr
|
|
NM_001360.3:c.1390G>A
MANE Select
|
NP_001351.2:p.Ala464Thr
|
|