ENST00000234071.8:c.1069A>T
MANE Select
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ENSP00000234071.4:p.Thr357Ser
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ENST00000234071.7:c.1069A>T
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ENSP00000234071.3:p.Thr357Ser
|
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ENST00000402125.2:c.393A>T
|
|
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ENST00000409048.1:c.1171A>T
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ENSP00000386679.1:p.Thr391Ser
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NM_000312.3:c.1069A>T , LRG_599t1:c.1069A>T
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NP_000303.1:p.Thr357Ser
|
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XM_005263715.3:c.1252A>T
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XP_005263772.1:p.Thr418Ser
|
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XM_005263716.3:c.1234A>T
|
XP_005263773.1:p.Thr412Ser
|
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XM_005263717.3:c.1132A>T
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XP_005263774.1:p.Thr378Ser
|
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XR_923313.1:n.1332-365T>A
|
|
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XM_005263717.4:c.1132A>T
|
XP_005263774.1:p.Thr378Ser
|
|
XM_017004505.1:c.1312A>T
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XP_016859994.1:p.Thr438Ser
|
|
XM_024453002.1:c.1414A>T
|
XP_024308770.1:p.Thr472Ser
|
|
XM_024453003.1:c.1354A>T
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XP_024308771.1:p.Thr452Ser
|
|
XM_024453004.1:c.1252A>T
|
XP_024308772.1:p.Thr418Ser
|
|
XM_024453005.1:c.1234A>T
|
XP_024308773.1:p.Thr412Ser
|
|
XM_024453006.1:c.1171A>T
|
XP_024308774.1:p.Thr391Ser
|
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XR_001739705.1:n.3607-365T>A
|
|
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XR_923313.2:n.4043-365T>A
|
|
|
NM_000312.4:c.1069A>T
MANE Select
|
NP_000303.1:p.Thr357Ser
|
|
NM_001375602.1:c.1252A>T
|
NP_001362531.1:p.Thr418Ser
|
|
NM_001375603.1:c.1234A>T
|
NP_001362532.1:p.Thr412Ser
|
|
NM_001375604.1:c.1132A>T
|
NP_001362533.1:p.Thr378Ser
|
|
NM_001375605.1:c.1171A>T
|
NP_001362534.1:p.Thr391Ser
|
|
NM_001375606.1:c.1237A>T
|
NP_001362535.1:p.Thr413Ser
|
|
NM_001375607.1:c.1255A>T
|
NP_001362536.1:p.Thr419Ser
|
|
NM_001375608.1:c.1012A>T
|
NP_001362537.1:p.Thr338Ser
|
|
NM_001375609.1:c.1045A>T
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NP_001362538.1:p.Thr349Ser
|
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NM_001375610.1:c.1063A>T
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NP_001362539.1:p.Thr355Ser
|
|
NM_001375611.1:c.1069A>T
|
NP_001362540.1:p.Thr357Ser
|
|
NM_001375613.1:c.1069A>T
|
NP_001362542.1:p.Thr357Ser
|
|