ENST00000234071.8:c.1008G>T
MANE Select
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ENSP00000234071.4:p.Glu336Asp
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ENST00000234071.7:c.1008G>T
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ENSP00000234071.3:p.Glu336Asp
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ENST00000402125.2:c.332G>T
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ENST00000409048.1:c.1110G>T
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ENSP00000386679.1:p.Glu370Asp
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NM_000312.3:c.1008G>T , LRG_599t1:c.1008G>T
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NP_000303.1:p.Glu336Asp
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XM_005263715.3:c.1191G>T
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XP_005263772.1:p.Glu397Asp
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XM_005263716.3:c.1173G>T
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XP_005263773.1:p.Glu391Asp
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XM_005263717.3:c.1071G>T
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XP_005263774.1:p.Glu357Asp
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XR_923313.1:n.1332-304C>A
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XM_005263717.4:c.1071G>T
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XP_005263774.1:p.Glu357Asp
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XM_017004505.1:c.1251G>T
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XP_016859994.1:p.Glu417Asp
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XM_024453002.1:c.1353G>T
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XP_024308770.1:p.Glu451Asp
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XM_024453003.1:c.1293G>T
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XP_024308771.1:p.Glu431Asp
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XM_024453004.1:c.1191G>T
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XP_024308772.1:p.Glu397Asp
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XM_024453005.1:c.1173G>T
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XP_024308773.1:p.Glu391Asp
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XM_024453006.1:c.1110G>T
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XP_024308774.1:p.Glu370Asp
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XR_001739705.1:n.3607-304C>A
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XR_923313.2:n.4043-304C>A
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NM_000312.4:c.1008G>T
MANE Select
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NP_000303.1:p.Glu336Asp
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NM_001375602.1:c.1191G>T
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NP_001362531.1:p.Glu397Asp
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NM_001375603.1:c.1173G>T
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NP_001362532.1:p.Glu391Asp
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NM_001375604.1:c.1071G>T
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NP_001362533.1:p.Glu357Asp
|
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NM_001375605.1:c.1110G>T
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NP_001362534.1:p.Glu370Asp
|
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NM_001375606.1:c.1176G>T
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NP_001362535.1:p.Glu392Asp
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NM_001375607.1:c.1194G>T
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NP_001362536.1:p.Glu398Asp
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NM_001375608.1:c.951G>T
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NP_001362537.1:p.Glu317Asp
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NM_001375609.1:c.984G>T
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NP_001362538.1:p.Glu328Asp
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NM_001375610.1:c.1002G>T
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NP_001362539.1:p.Glu334Asp
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NM_001375611.1:c.1008G>T
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NP_001362540.1:p.Glu336Asp
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NM_001375613.1:c.1008G>T
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NP_001362542.1:p.Glu336Asp
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