ENST00000525346.6:c.971A>G
|
ENSP00000435707.3:p.Tyr324Cys
|
|
ENST00000526780.6:c.971A>G
|
ENSP00000435668.2:p.Tyr324Cys
|
|
ENST00000527316.6:c.797A>G
|
ENSP00000435047.2:p.Tyr266Cys
|
|
ENST00000682708.1:c.1022A>G
|
ENSP00000506866.1:p.Tyr341Cys
|
|
ENST00000683287.1:c.1007A>G
|
ENSP00000507607.1:p.Tyr336Cys
|
|
ENST00000683714.1:c.979A>G
|
ENSP00000508207.1:p.Thr327Ala
|
|
ENST00000684396.1:n.1011A>G
|
|
|
ENST00000685320.1:c.386A>G
|
ENSP00000509319.1:p.Tyr129Cys
|
|
ENST00000690257.1:c.875A>G
|
ENSP00000510750.1:p.Tyr292Cys
|
|
ENST00000355527.8:c.971A>G
MANE Select
|
ENSP00000347717.4:p.Tyr324Cys
|
|
ENST00000355527.7:c.971A>G
|
ENSP00000347717.3:p.Tyr324Cys
|
|
ENST00000407721.6:c.971A>G
|
ENSP00000384739.2:p.Tyr324Cys
|
|
ENST00000525137.1:c.472A>G
|
ENSP00000435956.1:p.Thr158Ala
|
|
ENST00000533800.5:c.221A>G
|
ENSP00000435011.1:p.Tyr74Cys
|
|
ENST00000534795.5:c.319+1980A>G
|
|
|
NM_001163817.1:c.971A>G
|
NP_001157289.1:p.Tyr324Cys
|
|
NM_001360.2:c.971A>G , LRG_340t1:c.971A>G
|
NP_001351.2:p.Tyr324Cys
|
|
XM_011544777.1:c.1105A>G
|
XP_011543079.1:p.Thr369Ala
|
|
XM_011544777.2:c.1105A>G
|
XP_011543079.1:p.Thr369Ala
|
|
NM_001163817.2:c.971A>G
|
NP_001157289.1:p.Tyr324Cys
|
|
NM_001360.3:c.971A>G
MANE Select
|
NP_001351.2:p.Tyr324Cys
|
|