ENST00000318471.5:c.873T>C
MANE Select
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ENSP00000315680.3:p.Gly291=
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ENST00000541292.6:c.*138T>C
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ENSP00000441004.1:n.*138T>C
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ENST00000678002.1:c.561T>C
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ENST00000678557.1:c.759T>C
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ENSP00000502962.1:p.Gly253=
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ENST00000679286.1:c.753T>C
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ENSP00000503168.1:p.Gly251=
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ENST00000318471.4:c.873T>C
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ENSP00000315680.3:p.Gly291=
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NM_000288.3:c.873T>C
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NP_000279.1:p.Gly291=
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XM_005267019.3:c.759T>C
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XP_005267076.1:p.Gly253=
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XM_006715502.1:c.579T>C
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XP_006715565.1:p.Gly193=
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XM_011535900.1:c.596T>C
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XP_011534202.1:p.Val199Ala
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XM_005267019.4:c.759T>C
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XP_005267076.1:p.Gly253=
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XM_006715502.2:c.579T>C
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XP_006715565.1:p.Gly193=
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XM_017010934.2:c.596T>C
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XP_016866423.1:p.Val199Ala
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NM_000288.4:c.873T>C
MANE Select
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NP_000279.1:p.Gly291=
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