ENST00000525346.6:c.1017C>T
|
ENSP00000435707.3:p.Gly339=
|
|
ENST00000526780.6:c.1017C>T
|
ENSP00000435668.2:p.Gly339=
|
|
ENST00000527316.6:c.843C>T
|
ENSP00000435047.2:p.Gly281=
|
|
ENST00000682708.1:c.1068C>T
|
ENSP00000506866.1:p.Gly356=
|
|
ENST00000683287.1:c.1053C>T
|
ENSP00000507607.1:p.Gly351=
|
|
ENST00000683714.1:c.1025C>T
|
ENSP00000508207.1:p.Ala342Val
|
|
ENST00000684396.1:n.1057C>T
|
|
|
ENST00000685320.1:c.432C>T
|
ENSP00000509319.1:p.Gly144=
|
|
ENST00000690257.1:c.921C>T
|
ENSP00000510750.1:p.Gly307=
|
|
ENST00000355527.8:c.1017C>T
MANE Select
|
ENSP00000347717.4:p.Gly339=
|
|
ENST00000355527.7:c.1017C>T
|
ENSP00000347717.3:p.Gly339=
|
|
ENST00000407721.6:c.1017C>T
|
ENSP00000384739.2:p.Gly339=
|
|
ENST00000525137.1:c.518C>T
|
ENSP00000435956.1:p.Ala173Val
|
|
ENST00000533800.5:c.267C>T
|
ENSP00000435011.1:p.Gly89=
|
|
ENST00000534795.5:c.319+2026C>T
|
|
|
NM_001163817.1:c.1017C>T
|
NP_001157289.1:p.Gly339=
|
|
NM_001360.2:c.1017C>T , LRG_340t1:c.1017C>T
|
NP_001351.2:p.Gly339=
|
|
XM_011544777.1:c.1151C>T
|
XP_011543079.1:p.Ala384Val
|
|
XM_011544777.2:c.1151C>T
|
XP_011543079.1:p.Ala384Val
|
|
NM_001163817.2:c.1017C>T
|
NP_001157289.1:p.Gly339=
|
|
NM_001360.3:c.1017C>T
MANE Select
|
NP_001351.2:p.Gly339=
|
|