ENST00000525346.6:c.1115G=
|
ENSP00000435707.3:p.Gly372=
|
|
ENST00000526780.6:c.1115G=
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ENSP00000435668.2:p.Gly372=
|
|
ENST00000527316.6:c.941G=
|
ENSP00000435047.2:p.Gly314=
|
|
ENST00000682708.1:c.1166G=
|
ENSP00000506866.1:p.Gly389=
|
|
ENST00000683287.1:c.1151G=
|
ENSP00000507607.1:p.Gly384=
|
|
ENST00000683714.1:c.1123G=
|
ENSP00000508207.1:p.Ala375=
|
|
ENST00000684396.1:n.1155G=
|
|
|
ENST00000685320.1:c.530G=
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ENSP00000509319.1:p.Gly177=
|
|
ENST00000690257.1:c.1019G=
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ENSP00000510750.1:p.Gly340=
|
|
ENST00000355527.8:c.1115G=
MANE Select
|
ENSP00000347717.4:p.Gly372=
|
|
ENST00000355527.7:c.1115G=
|
ENSP00000347717.3:p.Gly372=
|
|
ENST00000407721.6:c.1115G=
|
ENSP00000384739.2:p.Gly372=
|
|
ENST00000525137.1:c.616G=
|
ENSP00000435956.1:p.Ala206=
|
|
ENST00000533800.5:c.365G=
|
ENSP00000435011.1:p.Gly122=
|
|
ENST00000534795.5:c.319+2124G=
|
|
|
NM_001163817.1:c.1115G=
|
NP_001157289.1:p.Gly372=
|
|
NM_001360.2:c.1115G= , LRG_340t1:c.1115G=
|
NP_001351.2:p.Gly372=
|
|
XM_011544777.1:c.1249G=
|
XP_011543079.1:p.Ala417=
|
|
XM_011544777.2:c.1249G=
|
XP_011543079.1:p.Ala417=
|
|
NM_001163817.2:c.1115G=
|
NP_001157289.1:p.Gly372=
|
|
NM_001360.3:c.1115G=
MANE Select
|
NP_001351.2:p.Gly372=
|
|