ENST00000525346.6:c.1162C>T
|
ENSP00000435707.3:p.Gln388Ter
|
|
ENST00000526780.6:c.1162C>T
|
ENSP00000435668.2:p.Gln388Ter
|
|
ENST00000527316.6:c.988C>T
|
ENSP00000435047.2:p.Gln330Ter
|
|
ENST00000682708.1:c.1213C>T
|
ENSP00000506866.1:p.Gln405Ter
|
|
ENST00000683287.1:c.1198C>T
|
ENSP00000507607.1:p.Gln400Ter
|
|
ENST00000683714.1:c.1170C>T
|
ENSP00000508207.1:p.Gly390=
|
|
ENST00000684396.1:n.1202C>T
|
|
|
ENST00000685320.1:c.577C>T
|
ENSP00000509319.1:p.Gln193Ter
|
|
ENST00000690257.1:c.1066C>T
|
ENSP00000510750.1:p.Gln356Ter
|
|
ENST00000355527.8:c.1162C>T
MANE Select
|
ENSP00000347717.4:p.Gln388Ter
|
|
ENST00000355527.7:c.1162C>T
|
ENSP00000347717.3:p.Gln388Ter
|
|
ENST00000407721.6:c.1162C>T
|
ENSP00000384739.2:p.Gln388Ter
|
|
ENST00000525137.1:c.663C>T
|
ENSP00000435956.1:p.Gly221=
|
|
ENST00000533800.5:c.412C>T
|
ENSP00000435011.1:p.Gln138Ter
|
|
ENST00000534795.5:c.319+2171C>T
|
|
|
NM_001163817.1:c.1162C>T
|
NP_001157289.1:p.Gln388Ter
|
|
NM_001360.2:c.1162C>T , LRG_340t1:c.1162C>T
|
NP_001351.2:p.Gln388Ter
|
|
XM_011544777.1:c.1296C>T
|
XP_011543079.1:p.Gly432=
|
|
XM_011544777.2:c.1296C>T
|
XP_011543079.1:p.Gly432=
|
|
NM_001163817.2:c.1162C>T
|
NP_001157289.1:p.Gln388Ter
|
|
NM_001360.3:c.1162C>T
MANE Select
|
NP_001351.2:p.Gln388Ter
|
|