ENST00000234071.8:c.979G=
MANE Select
|
ENSP00000234071.4:p.Glu327=
|
|
ENST00000234071.7:c.979G=
|
ENSP00000234071.3:p.Glu327=
|
|
ENST00000402125.2:c.303G=
|
|
|
ENST00000409048.1:c.1081G=
|
ENSP00000386679.1:p.Glu361=
|
|
NM_000312.3:c.979G= , LRG_599t1:c.979G=
|
NP_000303.1:p.Glu327=
|
|
XM_005263715.3:c.1162G=
|
XP_005263772.1:p.Glu388=
|
|
XM_005263716.3:c.1144G=
|
XP_005263773.1:p.Glu382=
|
|
XM_005263717.3:c.1042G=
|
XP_005263774.1:p.Glu348=
|
|
XR_923313.1:n.1332-275C=
|
|
|
XM_005263717.4:c.1042G=
|
XP_005263774.1:p.Glu348=
|
|
XM_017004505.1:c.1222G=
|
XP_016859994.1:p.Glu408=
|
|
XM_024453002.1:c.1324G=
|
XP_024308770.1:p.Glu442=
|
|
XM_024453003.1:c.1264G=
|
XP_024308771.1:p.Glu422=
|
|
XM_024453004.1:c.1162G=
|
XP_024308772.1:p.Glu388=
|
|
XM_024453005.1:c.1144G=
|
XP_024308773.1:p.Glu382=
|
|
XM_024453006.1:c.1081G=
|
XP_024308774.1:p.Glu361=
|
|
XR_001739705.1:n.3607-275C=
|
|
|
XR_923313.2:n.4043-275C=
|
|
|
NM_000312.4:c.979G=
MANE Select
|
NP_000303.1:p.Glu327=
|
|
NM_001375602.1:c.1162G=
|
NP_001362531.1:p.Glu388=
|
|
NM_001375603.1:c.1144G=
|
NP_001362532.1:p.Glu382=
|
|
NM_001375604.1:c.1042G=
|
NP_001362533.1:p.Glu348=
|
|
NM_001375605.1:c.1081G=
|
NP_001362534.1:p.Glu361=
|
|
NM_001375606.1:c.1147G=
|
NP_001362535.1:p.Glu383=
|
|
NM_001375607.1:c.1165G=
|
NP_001362536.1:p.Glu389=
|
|
NM_001375608.1:c.922G=
|
NP_001362537.1:p.Glu308=
|
|
NM_001375609.1:c.955G=
|
NP_001362538.1:p.Glu319=
|
|
NM_001375610.1:c.973G=
|
NP_001362539.1:p.Glu325=
|
|
NM_001375611.1:c.979G=
|
NP_001362540.1:p.Glu327=
|
|
NM_001375613.1:c.979G=
|
NP_001362542.1:p.Glu327=
|
|