ENST00000525346.6:c.993G>C
|
ENSP00000435707.3:p.Gln331His
|
|
ENST00000526780.6:c.993G>C
|
ENSP00000435668.2:p.Gln331His
|
|
ENST00000527316.6:c.819G>C
|
ENSP00000435047.2:p.Gln273His
|
|
ENST00000682708.1:c.1044G>C
|
ENSP00000506866.1:p.Gln348His
|
|
ENST00000683287.1:c.1029G>C
|
ENSP00000507607.1:p.Gln343His
|
|
ENST00000683714.1:c.1001G>C
|
ENSP00000508207.1:p.Ser334Thr
|
|
ENST00000684396.1:n.1033G>C
|
|
|
ENST00000685320.1:c.408G>C
|
ENSP00000509319.1:p.Gln136His
|
|
ENST00000690257.1:c.897G>C
|
ENSP00000510750.1:p.Gln299His
|
|
ENST00000355527.8:c.993G>C
MANE Select
|
ENSP00000347717.4:p.Gln331His
|
|
ENST00000355527.7:c.993G>C
|
ENSP00000347717.3:p.Gln331His
|
|
ENST00000407721.6:c.993G>C
|
ENSP00000384739.2:p.Gln331His
|
|
ENST00000525137.1:c.494G>C
|
ENSP00000435956.1:p.Ser165Thr
|
|
ENST00000533800.5:c.243G>C
|
ENSP00000435011.1:p.Gln81His
|
|
ENST00000534795.5:c.319+2002G>C
|
|
|
NM_001163817.1:c.993G>C
|
NP_001157289.1:p.Gln331His
|
|
NM_001360.2:c.993G>C , LRG_340t1:c.993G>C
|
NP_001351.2:p.Gln331His
|
|
XM_011544777.1:c.1127G>C
|
XP_011543079.1:p.Ser376Thr
|
|
XM_011544777.2:c.1127G>C
|
XP_011543079.1:p.Ser376Thr
|
|
NM_001163817.2:c.993G>C
|
NP_001157289.1:p.Gln331His
|
|
NM_001360.3:c.993G>C
MANE Select
|
NP_001351.2:p.Gln331His
|
|