ENST00000525346.6:c.920G>C
|
ENSP00000435707.3:p.Gly307Ala
|
|
ENST00000526780.6:c.920G>C
|
ENSP00000435668.2:p.Gly307Ala
|
|
ENST00000527316.6:c.746G>C
|
ENSP00000435047.2:p.Gly249Ala
|
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ENST00000682708.1:c.971G>C
|
ENSP00000506866.1:p.Gly324Ala
|
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ENST00000682880.1:c.920G>C
|
ENSP00000507520.1:p.Gly307Ala
|
|
ENST00000683287.1:c.956G>C
|
ENSP00000507607.1:p.Gly319Ala
|
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ENST00000683714.1:c.920G>C
|
ENSP00000508207.1:p.Gly307Ala
|
|
ENST00000684396.1:n.960G>C
|
|
|
ENST00000685320.1:c.335G>C
|
ENSP00000509319.1:p.Gly112Ala
|
|
ENST00000690257.1:c.824G>C
|
ENSP00000510750.1:p.Gly275Ala
|
|
ENST00000355527.8:c.920G>C
MANE Select
|
ENSP00000347717.4:p.Gly307Ala
|
|
ENST00000355527.7:c.920G>C
|
ENSP00000347717.3:p.Gly307Ala
|
|
ENST00000407721.6:c.920G>C
|
ENSP00000384739.2:p.Gly307Ala
|
|
ENST00000525137.1:c.287G>C
|
ENSP00000435956.1:p.Gly96Ala
|
|
ENST00000533800.5:c.170G>C
|
ENSP00000435011.1:p.Gly57Ala
|
|
ENST00000534795.5:c.276G>C
|
|
|
NM_001163817.1:c.920G>C
|
NP_001157289.1:p.Gly307Ala
|
|
NM_001360.2:c.920G>C , LRG_340t1:c.920G>C
|
NP_001351.2:p.Gly307Ala
|
|
XM_011544777.1:c.920G>C
|
XP_011543079.1:p.Gly307Ala
|
|
XM_011544777.2:c.920G>C
|
XP_011543079.1:p.Gly307Ala
|
|
NM_001163817.2:c.920G>C
|
NP_001157289.1:p.Gly307Ala
|
|
NM_001360.3:c.920G>C
MANE Select
|
NP_001351.2:p.Gly307Ala
|
|