ENST00000318471.5:c.878A>G
MANE Select
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ENSP00000315680.3:p.Asp293Gly
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ENST00000541292.6:c.*143A>G
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ENSP00000441004.1:n.*143A>G
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ENST00000678002.1:c.566A>G
|
|
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ENST00000678557.1:c.764A>G
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ENSP00000502962.1:p.Asp255Gly
|
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ENST00000679286.1:c.758A>G
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ENSP00000503168.1:p.Asp253Gly
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ENST00000318471.4:c.878A>G
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ENSP00000315680.3:p.Asp293Gly
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NM_000288.3:c.878A>G
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NP_000279.1:p.Asp293Gly
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XM_005267019.3:c.764A>G
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XP_005267076.1:p.Asp255Gly
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XM_006715502.1:c.584A>G
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XP_006715565.1:p.Asp195Gly
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XM_011535900.1:c.*1A>G
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XP_011534202.1:n.*1A>G
|
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XM_005267019.4:c.764A>G
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XP_005267076.1:p.Asp255Gly
|
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XM_006715502.2:c.584A>G
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XP_006715565.1:p.Asp195Gly
|
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XM_017010934.2:c.*1A>G
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XP_016866423.1:n.*1A>G
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NM_000288.4:c.878A>G
MANE Select
|
NP_000279.1:p.Asp293Gly
|
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