ENST00000525346.6:c.1099C>G
|
ENSP00000435707.3:p.Arg367Gly
|
|
ENST00000526780.6:c.1099C>G
|
ENSP00000435668.2:p.Arg367Gly
|
|
ENST00000527316.6:c.925C>G
|
ENSP00000435047.2:p.Arg309Gly
|
|
ENST00000682708.1:c.1150C>G
|
ENSP00000506866.1:p.Arg384Gly
|
|
ENST00000683287.1:c.1135C>G
|
ENSP00000507607.1:p.Arg379Gly
|
|
ENST00000683714.1:c.1107C>G
|
ENSP00000508207.1:p.Gly369=
|
|
ENST00000684396.1:n.1139C>G
|
|
|
ENST00000685320.1:c.514C>G
|
ENSP00000509319.1:p.Arg172Gly
|
|
ENST00000690257.1:c.1003C>G
|
ENSP00000510750.1:p.Arg335Gly
|
|
ENST00000355527.8:c.1099C>G
MANE Select
|
ENSP00000347717.4:p.Arg367Gly
|
|
ENST00000355527.7:c.1099C>G
|
ENSP00000347717.3:p.Arg367Gly
|
|
ENST00000407721.6:c.1099C>G
|
ENSP00000384739.2:p.Arg367Gly
|
|
ENST00000525137.1:c.600C>G
|
ENSP00000435956.1:p.Gly200=
|
|
ENST00000533800.5:c.349C>G
|
ENSP00000435011.1:p.Arg117Gly
|
|
ENST00000534795.5:c.319+2108C>G
|
|
|
NM_001163817.1:c.1099C>G
|
NP_001157289.1:p.Arg367Gly
|
|
NM_001360.2:c.1099C>G , LRG_340t1:c.1099C>G
|
NP_001351.2:p.Arg367Gly
|
|
XM_011544777.1:c.1233C>G
|
XP_011543079.1:p.Gly411=
|
|
XM_011544777.2:c.1233C>G
|
XP_011543079.1:p.Gly411=
|
|
NM_001163817.2:c.1099C>G
|
NP_001157289.1:p.Arg367Gly
|
|
NM_001360.3:c.1099C>G
MANE Select
|
NP_001351.2:p.Arg367Gly
|
|