ENST00000234071.8:c.979G>A
MANE Select
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ENSP00000234071.4:p.Glu327Lys
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ENST00000234071.7:c.979G>A
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ENSP00000234071.3:p.Glu327Lys
|
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ENST00000402125.2:c.303G>A
|
|
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ENST00000409048.1:c.1081G>A
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ENSP00000386679.1:p.Glu361Lys
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NM_000312.3:c.979G>A , LRG_599t1:c.979G>A
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NP_000303.1:p.Glu327Lys
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XM_005263715.3:c.1162G>A
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XP_005263772.1:p.Glu388Lys
|
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XM_005263716.3:c.1144G>A
|
XP_005263773.1:p.Glu382Lys
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XM_005263717.3:c.1042G>A
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XP_005263774.1:p.Glu348Lys
|
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XR_923313.1:n.1332-275C>T
|
|
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XM_005263717.4:c.1042G>A
|
XP_005263774.1:p.Glu348Lys
|
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XM_017004505.1:c.1222G>A
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XP_016859994.1:p.Glu408Lys
|
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XM_024453002.1:c.1324G>A
|
XP_024308770.1:p.Glu442Lys
|
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XM_024453003.1:c.1264G>A
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XP_024308771.1:p.Glu422Lys
|
|
XM_024453004.1:c.1162G>A
|
XP_024308772.1:p.Glu388Lys
|
|
XM_024453005.1:c.1144G>A
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XP_024308773.1:p.Glu382Lys
|
|
XM_024453006.1:c.1081G>A
|
XP_024308774.1:p.Glu361Lys
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XR_001739705.1:n.3607-275C>T
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|
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XR_923313.2:n.4043-275C>T
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|
|
NM_000312.4:c.979G>A
MANE Select
|
NP_000303.1:p.Glu327Lys
|
|
NM_001375602.1:c.1162G>A
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NP_001362531.1:p.Glu388Lys
|
|
NM_001375603.1:c.1144G>A
|
NP_001362532.1:p.Glu382Lys
|
|
NM_001375604.1:c.1042G>A
|
NP_001362533.1:p.Glu348Lys
|
|
NM_001375605.1:c.1081G>A
|
NP_001362534.1:p.Glu361Lys
|
|
NM_001375606.1:c.1147G>A
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NP_001362535.1:p.Glu383Lys
|
|
NM_001375607.1:c.1165G>A
|
NP_001362536.1:p.Glu389Lys
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NM_001375608.1:c.922G>A
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NP_001362537.1:p.Glu308Lys
|
|
NM_001375609.1:c.955G>A
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NP_001362538.1:p.Glu319Lys
|
|
NM_001375610.1:c.973G>A
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NP_001362539.1:p.Glu325Lys
|
|
NM_001375611.1:c.979G>A
|
NP_001362540.1:p.Glu327Lys
|
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NM_001375613.1:c.979G>A
|
NP_001362542.1:p.Glu327Lys
|
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