ENST00000234071.8:c.1295A>T
MANE Select
|
ENSP00000234071.4:p.Tyr432Phe
|
|
ENST00000234071.7:c.1295A>T
|
ENSP00000234071.3:p.Tyr432Phe
|
|
ENST00000402125.2:c.619A>T
|
|
|
ENST00000409048.1:c.1397A>T
|
ENSP00000386679.1:p.Tyr466Phe
|
|
NM_000312.3:c.1295A>T , LRG_599t1:c.1295A>T
|
NP_000303.1:p.Tyr432Phe
|
|
XM_005263715.3:c.1478A>T
|
XP_005263772.1:p.Tyr493Phe
|
|
XM_005263716.3:c.1460A>T
|
XP_005263773.1:p.Tyr487Phe
|
|
XM_005263717.3:c.1358A>T
|
XP_005263774.1:p.Tyr453Phe
|
|
XR_923313.1:n.1332-591T>A
|
|
|
XM_005263717.4:c.1358A>T
|
XP_005263774.1:p.Tyr453Phe
|
|
XM_017004505.1:c.1538A>T
|
XP_016859994.1:p.Tyr513Phe
|
|
XM_024453002.1:c.1640A>T
|
XP_024308770.1:p.Tyr547Phe
|
|
XM_024453003.1:c.1580A>T
|
XP_024308771.1:p.Tyr527Phe
|
|
XM_024453004.1:c.1478A>T
|
XP_024308772.1:p.Tyr493Phe
|
|
XM_024453005.1:c.1460A>T
|
XP_024308773.1:p.Tyr487Phe
|
|
XM_024453006.1:c.1397A>T
|
XP_024308774.1:p.Tyr466Phe
|
|
XR_001739705.1:n.3607-591T>A
|
|
|
XR_923313.2:n.4043-591T>A
|
|
|
NM_000312.4:c.1295A>T
MANE Select
|
NP_000303.1:p.Tyr432Phe
|
|
NM_001375602.1:c.1478A>T
|
NP_001362531.1:p.Tyr493Phe
|
|
NM_001375603.1:c.1460A>T
|
NP_001362532.1:p.Tyr487Phe
|
|
NM_001375604.1:c.1358A>T
|
NP_001362533.1:p.Tyr453Phe
|
|
NM_001375605.1:c.1397A>T
|
NP_001362534.1:p.Tyr466Phe
|
|
NM_001375606.1:c.1463A>T
|
NP_001362535.1:p.Tyr488Phe
|
|
NM_001375607.1:c.1481A>T
|
NP_001362536.1:p.Tyr494Phe
|
|
NM_001375608.1:c.1238A>T
|
NP_001362537.1:p.Tyr413Phe
|
|
NM_001375609.1:c.1271A>T
|
NP_001362538.1:p.Tyr424Phe
|
|
NM_001375610.1:c.1289A>T
|
NP_001362539.1:p.Tyr430Phe
|
|
NM_001375611.1:c.1295A>T
|
NP_001362540.1:p.Tyr432Phe
|
|
NM_001375613.1:c.1295A>T
|
NP_001362542.1:p.Tyr432Phe
|
|