ENST00000318158.11:c.527G>C
MANE Select
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ENSP00000313432.6:p.Gly176Ala
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ENST00000318158.10:c.527G>C
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ENSP00000313432.6:p.Gly176Ala
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ENST00000377824.8:n.564G>C
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ENST00000460882.5:n.554G>C
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ENST00000480596.5:n.1228G>C
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ENST00000491488.5:n.232G>C
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ENST00000494290.1:c.98G>C
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ENSP00000432021.1:p.Gly33Ala
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ENST00000497693.1:n.2060G>C
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ENST00000607784.1:c.527G>C
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ENSP00000475569.1:p.Gly176Ala
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NM_012203.1:c.527G>C
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NP_036335.1:p.Gly176Ala
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XM_005251631.1:c.206G>C
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XP_005251688.1:p.Gly69Ala
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XM_011518073.1:c.125G>C
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XP_011516375.1:p.Gly42Ala
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XR_929374.1:n.972G>C
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XM_017015320.2:c.527G>C
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XP_016870809.1:p.Gly176Ala
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XM_017015321.2:c.527G>C
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XP_016870810.1:p.Gly176Ala
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XM_017015323.2:c.125G>C
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XP_016870812.1:p.Gly42Ala
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XM_024447716.1:c.800G>C
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XP_024303484.1:p.Gly267Ala
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XM_024447717.1:c.800G>C
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XP_024303485.1:p.Gly267Ala
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XR_002956828.1:n.815G>C
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XR_002956829.1:n.815G>C
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XR_002956830.1:n.586G>C
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XR_002956831.1:n.261G>C
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XR_002956832.1:n.946G>C
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NM_012203.2:c.527G>C
MANE Select
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NP_036335.1:p.Gly176Ala
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