ENST00000234071.8:c.910C>T
MANE Select
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ENSP00000234071.4:p.His304Tyr
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ENST00000234071.7:c.910C>T
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ENSP00000234071.3:p.His304Tyr
|
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ENST00000402125.2:c.234C>T
|
|
|
ENST00000409048.1:c.1012C>T
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ENSP00000386679.1:p.His338Tyr
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NM_000312.3:c.910C>T , LRG_599t1:c.910C>T
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NP_000303.1:p.His304Tyr
|
|
XM_005263715.3:c.1093C>T
|
XP_005263772.1:p.His365Tyr
|
|
XM_005263716.3:c.1075C>T
|
XP_005263773.1:p.His359Tyr
|
|
XM_005263717.3:c.973C>T
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XP_005263774.1:p.His325Tyr
|
|
XR_923313.1:n.1332-206G>A
|
|
|
XM_005263717.4:c.973C>T
|
XP_005263774.1:p.His325Tyr
|
|
XM_017004505.1:c.1153C>T
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XP_016859994.1:p.His385Tyr
|
|
XM_024453002.1:c.1255C>T
|
XP_024308770.1:p.His419Tyr
|
|
XM_024453003.1:c.1195C>T
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XP_024308771.1:p.His399Tyr
|
|
XM_024453004.1:c.1093C>T
|
XP_024308772.1:p.His365Tyr
|
|
XM_024453005.1:c.1075C>T
|
XP_024308773.1:p.His359Tyr
|
|
XM_024453006.1:c.1012C>T
|
XP_024308774.1:p.His338Tyr
|
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XR_001739705.1:n.3607-206G>A
|
|
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XR_923313.2:n.4043-206G>A
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|
|
NM_000312.4:c.910C>T
MANE Select
|
NP_000303.1:p.His304Tyr
|
|
NM_001375602.1:c.1093C>T
|
NP_001362531.1:p.His365Tyr
|
|
NM_001375603.1:c.1075C>T
|
NP_001362532.1:p.His359Tyr
|
|
NM_001375604.1:c.973C>T
|
NP_001362533.1:p.His325Tyr
|
|
NM_001375605.1:c.1012C>T
|
NP_001362534.1:p.His338Tyr
|
|
NM_001375606.1:c.1078C>T
|
NP_001362535.1:p.His360Tyr
|
|
NM_001375607.1:c.1096C>T
|
NP_001362536.1:p.His366Tyr
|
|
NM_001375608.1:c.853C>T
|
NP_001362537.1:p.His285Tyr
|
|
NM_001375609.1:c.886C>T
|
NP_001362538.1:p.His296Tyr
|
|
NM_001375610.1:c.904C>T
|
NP_001362539.1:p.His302Tyr
|
|
NM_001375611.1:c.910C>T
|
NP_001362540.1:p.His304Tyr
|
|
NM_001375613.1:c.910C>T
|
NP_001362542.1:p.His304Tyr
|
|