ENST00000234071.8:c.1006G>T
MANE Select
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ENSP00000234071.4:p.Glu336Ter
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ENST00000234071.7:c.1006G>T
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ENSP00000234071.3:p.Glu336Ter
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ENST00000402125.2:c.330G>T
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ENST00000409048.1:c.1108G>T
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ENSP00000386679.1:p.Glu370Ter
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NM_000312.3:c.1006G>T , LRG_599t1:c.1006G>T
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NP_000303.1:p.Glu336Ter
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XM_005263715.3:c.1189G>T
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XP_005263772.1:p.Glu397Ter
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XM_005263716.3:c.1171G>T
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XP_005263773.1:p.Glu391Ter
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XM_005263717.3:c.1069G>T
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XP_005263774.1:p.Glu357Ter
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XR_923313.1:n.1332-302C>A
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XM_005263717.4:c.1069G>T
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XP_005263774.1:p.Glu357Ter
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XM_017004505.1:c.1249G>T
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XP_016859994.1:p.Glu417Ter
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XM_024453002.1:c.1351G>T
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XP_024308770.1:p.Glu451Ter
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XM_024453003.1:c.1291G>T
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XP_024308771.1:p.Glu431Ter
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XM_024453004.1:c.1189G>T
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XP_024308772.1:p.Glu397Ter
|
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XM_024453005.1:c.1171G>T
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XP_024308773.1:p.Glu391Ter
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XM_024453006.1:c.1108G>T
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XP_024308774.1:p.Glu370Ter
|
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XR_001739705.1:n.3607-302C>A
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XR_923313.2:n.4043-302C>A
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|
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NM_000312.4:c.1006G>T
MANE Select
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NP_000303.1:p.Glu336Ter
|
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NM_001375602.1:c.1189G>T
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NP_001362531.1:p.Glu397Ter
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NM_001375603.1:c.1171G>T
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NP_001362532.1:p.Glu391Ter
|
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NM_001375604.1:c.1069G>T
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NP_001362533.1:p.Glu357Ter
|
|
NM_001375605.1:c.1108G>T
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NP_001362534.1:p.Glu370Ter
|
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NM_001375606.1:c.1174G>T
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NP_001362535.1:p.Glu392Ter
|
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NM_001375607.1:c.1192G>T
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NP_001362536.1:p.Glu398Ter
|
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NM_001375608.1:c.949G>T
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NP_001362537.1:p.Glu317Ter
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NM_001375609.1:c.982G>T
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NP_001362538.1:p.Glu328Ter
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NM_001375610.1:c.1000G>T
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NP_001362539.1:p.Glu334Ter
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|
NM_001375611.1:c.1006G>T
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NP_001362540.1:p.Glu336Ter
|
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NM_001375613.1:c.1006G>T
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NP_001362542.1:p.Glu336Ter
|
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