ENST00000234071.8:c.978A>T
MANE Select
|
ENSP00000234071.4:p.Ala326=
|
|
ENST00000234071.7:c.978A>T
|
ENSP00000234071.3:p.Ala326=
|
|
ENST00000402125.2:c.302A>T
|
|
|
ENST00000409048.1:c.1080A>T
|
ENSP00000386679.1:p.Ala360=
|
|
NM_000312.3:c.978A>T , LRG_599t1:c.978A>T
|
NP_000303.1:p.Ala326=
|
|
XM_005263715.3:c.1161A>T
|
XP_005263772.1:p.Ala387=
|
|
XM_005263716.3:c.1143A>T
|
XP_005263773.1:p.Ala381=
|
|
XM_005263717.3:c.1041A>T
|
XP_005263774.1:p.Ala347=
|
|
XR_923313.1:n.1332-274T>A
|
|
|
XM_005263717.4:c.1041A>T
|
XP_005263774.1:p.Ala347=
|
|
XM_017004505.1:c.1221A>T
|
XP_016859994.1:p.Ala407=
|
|
XM_024453002.1:c.1323A>T
|
XP_024308770.1:p.Ala441=
|
|
XM_024453003.1:c.1263A>T
|
XP_024308771.1:p.Ala421=
|
|
XM_024453004.1:c.1161A>T
|
XP_024308772.1:p.Ala387=
|
|
XM_024453005.1:c.1143A>T
|
XP_024308773.1:p.Ala381=
|
|
XM_024453006.1:c.1080A>T
|
XP_024308774.1:p.Ala360=
|
|
XR_001739705.1:n.3607-274T>A
|
|
|
XR_923313.2:n.4043-274T>A
|
|
|
NM_000312.4:c.978A>T
MANE Select
|
NP_000303.1:p.Ala326=
|
|
NM_001375602.1:c.1161A>T
|
NP_001362531.1:p.Ala387=
|
|
NM_001375603.1:c.1143A>T
|
NP_001362532.1:p.Ala381=
|
|
NM_001375604.1:c.1041A>T
|
NP_001362533.1:p.Ala347=
|
|
NM_001375605.1:c.1080A>T
|
NP_001362534.1:p.Ala360=
|
|
NM_001375606.1:c.1146A>T
|
NP_001362535.1:p.Ala382=
|
|
NM_001375607.1:c.1164A>T
|
NP_001362536.1:p.Ala388=
|
|
NM_001375608.1:c.921A>T
|
NP_001362537.1:p.Ala307=
|
|
NM_001375609.1:c.954A>T
|
NP_001362538.1:p.Ala318=
|
|
NM_001375610.1:c.972A>T
|
NP_001362539.1:p.Ala324=
|
|
NM_001375611.1:c.978A>T
|
NP_001362540.1:p.Ala326=
|
|
NM_001375613.1:c.978A>T
|
NP_001362542.1:p.Ala326=
|
|