ENST00000234071.8:c.1142T>G
MANE Select
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ENSP00000234071.4:p.Val381Gly
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ENST00000234071.7:c.1142T>G
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ENSP00000234071.3:p.Val381Gly
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ENST00000402125.2:c.466T>G
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ENST00000409048.1:c.1244T>G
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ENSP00000386679.1:p.Val415Gly
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NM_000312.3:c.1142T>G , LRG_599t1:c.1142T>G
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NP_000303.1:p.Val381Gly
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XM_005263715.3:c.1325T>G
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XP_005263772.1:p.Val442Gly
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XM_005263716.3:c.1307T>G
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XP_005263773.1:p.Val436Gly
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XM_005263717.3:c.1205T>G
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XP_005263774.1:p.Val402Gly
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XR_923313.1:n.1332-438A>C
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XM_005263717.4:c.1205T>G
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XP_005263774.1:p.Val402Gly
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XM_017004505.1:c.1385T>G
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XP_016859994.1:p.Val462Gly
|
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XM_024453002.1:c.1487T>G
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XP_024308770.1:p.Val496Gly
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XM_024453003.1:c.1427T>G
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XP_024308771.1:p.Val476Gly
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XM_024453004.1:c.1325T>G
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XP_024308772.1:p.Val442Gly
|
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XM_024453005.1:c.1307T>G
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XP_024308773.1:p.Val436Gly
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XM_024453006.1:c.1244T>G
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XP_024308774.1:p.Val415Gly
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XR_001739705.1:n.3607-438A>C
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XR_923313.2:n.4043-438A>C
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NM_000312.4:c.1142T>G
MANE Select
|
NP_000303.1:p.Val381Gly
|
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NM_001375602.1:c.1325T>G
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NP_001362531.1:p.Val442Gly
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NM_001375603.1:c.1307T>G
|
NP_001362532.1:p.Val436Gly
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NM_001375604.1:c.1205T>G
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NP_001362533.1:p.Val402Gly
|
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NM_001375605.1:c.1244T>G
|
NP_001362534.1:p.Val415Gly
|
|
NM_001375606.1:c.1310T>G
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NP_001362535.1:p.Val437Gly
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NM_001375607.1:c.1328T>G
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NP_001362536.1:p.Val443Gly
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NM_001375608.1:c.1085T>G
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NP_001362537.1:p.Val362Gly
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NM_001375609.1:c.1118T>G
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NP_001362538.1:p.Val373Gly
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NM_001375610.1:c.1136T>G
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NP_001362539.1:p.Val379Gly
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NM_001375611.1:c.1142T>G
|
NP_001362540.1:p.Val381Gly
|
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NM_001375613.1:c.1142T>G
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NP_001362542.1:p.Val381Gly
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