ENST00000525346.6:c.1265G>T
|
ENSP00000435707.3:p.Cys422Phe
|
|
ENST00000526780.6:c.1265G>T
|
ENSP00000435668.2:p.Cys422Phe
|
|
ENST00000527316.6:c.1091G>T
|
ENSP00000435047.2:p.Cys364Phe
|
|
ENST00000682708.1:c.1316G>T
|
ENSP00000506866.1:p.Cys439Phe
|
|
ENST00000683287.1:c.1301G>T
|
ENSP00000507607.1:p.Cys434Phe
|
|
ENST00000683714.1:c.*28G>T
|
ENSP00000508207.1:n.*28G>T
|
|
ENST00000684396.1:n.1305G>T
|
|
|
ENST00000685320.1:c.680G>T
|
ENSP00000509319.1:p.Cys227Phe
|
|
ENST00000690257.1:c.1169G>T
|
ENSP00000510750.1:p.Cys390Phe
|
|
ENST00000355527.8:c.1265G>T
MANE Select
|
ENSP00000347717.4:p.Cys422Phe
|
|
ENST00000355527.7:c.1265G>T
|
ENSP00000347717.3:p.Cys422Phe
|
|
ENST00000407721.6:c.1265G>T
|
ENSP00000384739.2:p.Cys422Phe
|
|
ENST00000525137.1:c.766G>T
|
ENSP00000435956.1:n.766G>T
|
|
ENST00000533800.5:c.515G>T
|
ENSP00000435011.1:p.Cys172Phe
|
|
ENST00000534795.5:c.319+2274G>T
|
|
|
NM_001163817.1:c.1265G>T
|
NP_001157289.1:p.Cys422Phe
|
|
NM_001360.2:c.1265G>T , LRG_340t1:c.1265G>T
|
NP_001351.2:p.Cys422Phe
|
|
XM_011544777.1:c.*28G>T
|
XP_011543079.1:n.*28G>T
|
|
XM_011544777.2:c.*28G>T
|
XP_011543079.1:n.*28G>T
|
|
NM_001163817.2:c.1265G>T
|
NP_001157289.1:p.Cys422Phe
|
|
NM_001360.3:c.1265G>T
MANE Select
|
NP_001351.2:p.Cys422Phe
|
|