ENST00000234071.8:c.1195G=
MANE Select
|
ENSP00000234071.4:p.Glu399=
|
|
ENST00000234071.7:c.1195G=
|
ENSP00000234071.3:p.Glu399=
|
|
ENST00000402125.2:c.519G=
|
|
|
ENST00000409048.1:c.1297G=
|
ENSP00000386679.1:p.Glu433=
|
|
NM_000312.3:c.1195G= , LRG_599t1:c.1195G=
|
NP_000303.1:p.Glu399=
|
|
XM_005263715.3:c.1378G=
|
XP_005263772.1:p.Glu460=
|
|
XM_005263716.3:c.1360G=
|
XP_005263773.1:p.Glu454=
|
|
XM_005263717.3:c.1258G=
|
XP_005263774.1:p.Glu420=
|
|
XR_923313.1:n.1332-491C=
|
|
|
XM_005263717.4:c.1258G=
|
XP_005263774.1:p.Glu420=
|
|
XM_017004505.1:c.1438G=
|
XP_016859994.1:p.Glu480=
|
|
XM_024453002.1:c.1540G=
|
XP_024308770.1:p.Glu514=
|
|
XM_024453003.1:c.1480G=
|
XP_024308771.1:p.Glu494=
|
|
XM_024453004.1:c.1378G=
|
XP_024308772.1:p.Glu460=
|
|
XM_024453005.1:c.1360G=
|
XP_024308773.1:p.Glu454=
|
|
XM_024453006.1:c.1297G=
|
XP_024308774.1:p.Glu433=
|
|
XR_001739705.1:n.3607-491C=
|
|
|
XR_923313.2:n.4043-491C=
|
|
|
NM_000312.4:c.1195G=
MANE Select
|
NP_000303.1:p.Glu399=
|
|
NM_001375602.1:c.1378G=
|
NP_001362531.1:p.Glu460=
|
|
NM_001375603.1:c.1360G=
|
NP_001362532.1:p.Glu454=
|
|
NM_001375604.1:c.1258G=
|
NP_001362533.1:p.Glu420=
|
|
NM_001375605.1:c.1297G=
|
NP_001362534.1:p.Glu433=
|
|
NM_001375606.1:c.1363G=
|
NP_001362535.1:p.Glu455=
|
|
NM_001375607.1:c.1381G=
|
NP_001362536.1:p.Glu461=
|
|
NM_001375608.1:c.1138G=
|
NP_001362537.1:p.Glu380=
|
|
NM_001375609.1:c.1171G=
|
NP_001362538.1:p.Glu391=
|
|
NM_001375610.1:c.1189G=
|
NP_001362539.1:p.Glu397=
|
|
NM_001375611.1:c.1195G=
|
NP_001362540.1:p.Glu399=
|
|
NM_001375613.1:c.1195G=
|
NP_001362542.1:p.Glu399=
|
|