ENST00000370096.9:c.2639G>A
MANE Select
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ENSP00000359114.3:p.Gly880Asp
|
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ENST00000353414.8:c.2522G>A
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ENSP00000302551.6:p.Gly841Asp
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ENST00000358392.6:c.2675G>A
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ENSP00000351163.2:p.Gly892Asp
|
|
ENST00000370096.7:c.2639G>A
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ENSP00000359114.3:p.Gly880Asp
|
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ENST00000512756.5:c.2291G>A
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ENSP00000426533.1:p.Gly764Asp
|
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ENST00000635193.1:c.1973G>A
|
|
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NM_001190709.1:c.2522G>A
|
NP_001177638.1:p.Gly841Asp
|
|
NM_001854.3:c.2639G>A
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NP_001845.3:p.Gly880Asp
|
|
NM_080629.2:c.2675G>A
|
NP_542196.2:p.Gly892Asp
|
|
NM_080630.3:c.2291G>A
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NP_542197.3:p.Gly764Asp
|
|
XM_011540719.1:c.2639G>A
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XP_011539021.1:p.Gly880Asp
|
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XM_011540720.1:c.872G>A
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XP_011539022.1:p.Gly291Asp
|
|
XM_011540721.1:c.227G>A
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XP_011539023.1:p.Gly76Asp
|
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XR_946545.1:n.3053G>A
|
|
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NR_134980.1:n.2973G>A
|
|
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XM_017000334.1:c.2792G>A
|
XP_016855823.1:p.Gly931Asp
|
|
XM_017000335.1:c.2786G>A
|
XP_016855824.1:p.Gly929Asp
|
|
XM_017000336.1:c.2792G>A
|
XP_016855825.1:p.Gly931Asp
|
|
XM_017000337.1:c.1190G>A
|
XP_016855826.1:p.Gly397Asp
|
|
NM_001854.4:c.2639G>A
MANE Select
|
NP_001845.3:p.Gly880Asp
|
|
NM_080630.4:c.2291G>A
|
NP_542197.3:p.Gly764Asp
|
|
NR_134980.2:n.2999G>A
|
|
|
NM_001190709.2:c.2522G>A
|
NP_001177638.1:p.Gly841Asp
|
|
NM_080629.3:c.2675G>A
|
NP_542196.2:p.Gly892Asp
|
|