ENST00000525346.6:c.1274G>C
|
ENSP00000435707.3:p.Gly425Ala
|
|
ENST00000526780.6:c.1274G>C
|
ENSP00000435668.2:p.Gly425Ala
|
|
ENST00000527316.6:c.1100G>C
|
ENSP00000435047.2:p.Gly367Ala
|
|
ENST00000682708.1:c.1325G>C
|
ENSP00000506866.1:p.Gly442Ala
|
|
ENST00000683287.1:c.1310G>C
|
ENSP00000507607.1:p.Gly437Ala
|
|
ENST00000683714.1:c.*37G>C
|
ENSP00000508207.1:n.*37G>C
|
|
ENST00000684396.1:n.1314G>C
|
|
|
ENST00000685320.1:c.689G>C
|
ENSP00000509319.1:p.Gly230Ala
|
|
ENST00000690257.1:c.1178G>C
|
ENSP00000510750.1:p.Gly393Ala
|
|
ENST00000355527.8:c.1274G>C
MANE Select
|
ENSP00000347717.4:p.Gly425Ala
|
|
ENST00000355527.7:c.1274G>C
|
ENSP00000347717.3:p.Gly425Ala
|
|
ENST00000407721.6:c.1274G>C
|
ENSP00000384739.2:p.Gly425Ala
|
|
ENST00000525137.1:c.775G>C
|
ENSP00000435956.1:n.775G>C
|
|
ENST00000533800.5:c.524G>C
|
ENSP00000435011.1:p.Gly175Ala
|
|
ENST00000534795.5:c.319+2283G>C
|
|
|
NM_001163817.1:c.1274G>C
|
NP_001157289.1:p.Gly425Ala
|
|
NM_001360.2:c.1274G>C , LRG_340t1:c.1274G>C
|
NP_001351.2:p.Gly425Ala
|
|
XM_011544777.1:c.*37G>C
|
XP_011543079.1:n.*37G>C
|
|
XM_011544777.2:c.*37G>C
|
XP_011543079.1:n.*37G>C
|
|
NM_001163817.2:c.1274G>C
|
NP_001157289.1:p.Gly425Ala
|
|
NM_001360.3:c.1274G>C
MANE Select
|
NP_001351.2:p.Gly425Ala
|
|