ENST00000234071.8:c.1237A>T
MANE Select
|
ENSP00000234071.4:p.Thr413Ser
|
|
ENST00000234071.7:c.1237A>T
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ENSP00000234071.3:p.Thr413Ser
|
|
ENST00000402125.2:c.561A>T
|
|
|
ENST00000409048.1:c.1339A>T
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ENSP00000386679.1:p.Thr447Ser
|
|
NM_000312.3:c.1237A>T , LRG_599t1:c.1237A>T
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NP_000303.1:p.Thr413Ser
|
|
XM_005263715.3:c.1420A>T
|
XP_005263772.1:p.Thr474Ser
|
|
XM_005263716.3:c.1402A>T
|
XP_005263773.1:p.Thr468Ser
|
|
XM_005263717.3:c.1300A>T
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XP_005263774.1:p.Thr434Ser
|
|
XR_923313.1:n.1332-533T>A
|
|
|
XM_005263717.4:c.1300A>T
|
XP_005263774.1:p.Thr434Ser
|
|
XM_017004505.1:c.1480A>T
|
XP_016859994.1:p.Thr494Ser
|
|
XM_024453002.1:c.1582A>T
|
XP_024308770.1:p.Thr528Ser
|
|
XM_024453003.1:c.1522A>T
|
XP_024308771.1:p.Thr508Ser
|
|
XM_024453004.1:c.1420A>T
|
XP_024308772.1:p.Thr474Ser
|
|
XM_024453005.1:c.1402A>T
|
XP_024308773.1:p.Thr468Ser
|
|
XM_024453006.1:c.1339A>T
|
XP_024308774.1:p.Thr447Ser
|
|
XR_001739705.1:n.3607-533T>A
|
|
|
XR_923313.2:n.4043-533T>A
|
|
|
NM_000312.4:c.1237A>T
MANE Select
|
NP_000303.1:p.Thr413Ser
|
|
NM_001375602.1:c.1420A>T
|
NP_001362531.1:p.Thr474Ser
|
|
NM_001375603.1:c.1402A>T
|
NP_001362532.1:p.Thr468Ser
|
|
NM_001375604.1:c.1300A>T
|
NP_001362533.1:p.Thr434Ser
|
|
NM_001375605.1:c.1339A>T
|
NP_001362534.1:p.Thr447Ser
|
|
NM_001375606.1:c.1405A>T
|
NP_001362535.1:p.Thr469Ser
|
|
NM_001375607.1:c.1423A>T
|
NP_001362536.1:p.Thr475Ser
|
|
NM_001375608.1:c.1180A>T
|
NP_001362537.1:p.Thr394Ser
|
|
NM_001375609.1:c.1213A>T
|
NP_001362538.1:p.Thr405Ser
|
|
NM_001375610.1:c.1231A>T
|
NP_001362539.1:p.Thr411Ser
|
|
NM_001375611.1:c.1237A>T
|
NP_001362540.1:p.Thr413Ser
|
|
NM_001375613.1:c.1237A>T
|
NP_001362542.1:p.Thr413Ser
|
|