ENST00000262178.7:c.836T>G
MANE Select
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ENSP00000262178.2:p.Val279Gly
|
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ENST00000262178.6:c.836T>G
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ENSP00000262178.2:p.Val279Gly
|
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ENST00000377633.7:c.788T>G
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ENSP00000366860.3:p.Val263Gly
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ENST00000402066.5:c.1259T>G
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ENSP00000384497.1:p.Val420Gly
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NM_001304522.1:c.596T>G
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NP_001291451.1:p.Val199Gly
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NM_001308259.1:c.788T>G
|
NP_001295188.1:p.Val263Gly
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NM_003382.4:c.836T>G
|
NP_003373.2:p.Val279Gly
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NR_130758.1:n.1022T>G
|
|
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XM_005249561.2:c.911T>G
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XP_005249618.1:p.Val304Gly
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XM_006716107.1:c.836T>G
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XP_006716170.1:p.Val279Gly
|
|
XM_006716108.2:c.647T>G
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XP_006716171.1:p.Val216Gly
|
|
XM_011516550.1:c.788T>G
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XP_011514852.1:p.Val263Gly
|
|
XM_011516552.1:c.422T>G
|
XP_011514854.1:p.Val141Gly
|
|
XR_242047.2:n.1231T>G
|
|
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XM_005249561.3:c.911T>G
|
XP_005249618.1:p.Val304Gly
|
|
XM_006716107.2:c.836T>G
|
XP_006716170.1:p.Val279Gly
|
|
XM_006716108.3:c.647T>G
|
XP_006716171.1:p.Val216Gly
|
|
XM_011516550.2:c.788T>G
|
XP_011514852.1:p.Val263Gly
|
|
XM_017012580.1:c.422T>G
|
XP_016868069.1:p.Val141Gly
|
|
XM_024446914.1:c.911T>G
|
XP_024302682.1:p.Val304Gly
|
|
XM_024446915.1:c.911T>G
|
XP_024302683.1:p.Val304Gly
|
|
XM_024446916.1:c.836T>G
|
XP_024302684.1:p.Val279Gly
|
|
XM_024446917.1:c.647T>G
|
XP_024302685.1:p.Val216Gly
|
|
XM_024446918.1:c.422T>G
|
XP_024302686.1:p.Val141Gly
|
|
NM_003382.5:c.836T>G
MANE Select
|
NP_003373.2:p.Val279Gly
|
|
NM_001304522.2:c.596T>G
|
NP_001291451.1:p.Val199Gly
|
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NR_130758.2:n.932T>G
|
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