ENST00000281928.9:c.4980A>C
MANE Select
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ENSP00000281928.3:p.Gly1660=
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ENST00000549786.2:c.4408A>C
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ENST00000648379.1:n.3348A>C
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ENST00000648737.1:n.4744A>C
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ENST00000648825.1:n.1720A>C
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ENST00000648916.1:n.2991A>C
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ENST00000649146.1:n.2223A>C
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ENST00000649607.1:c.3164A>C
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ENST00000649775.1:c.1469A>C
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ENST00000650226.1:c.4980A>C
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ENSP00000496981.1:p.Gly1660=
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ENST00000281928.7:c.4980A>C
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ENSP00000281928.3:p.Gly1660=
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ENST00000549786.1:c.344A>C
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ENST00000552340.1:c.12A>C
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ENSP00000449876.1:p.Gly4=
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NM_015335.4:c.4980A>C
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NP_056150.1:p.Gly1660=
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XM_011538080.1:c.4980A>C
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XP_011536382.1:p.Gly1660=
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XM_011538081.1:c.4977A>C
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XP_011536383.1:p.Gly1659=
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XM_011538082.1:c.4950A>C
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XP_011536384.1:p.Gly1650=
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XM_011538080.2:c.4980A>C
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XP_011536382.1:p.Gly1660=
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XM_011538081.2:c.4977A>C
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XP_011536383.1:p.Gly1659=
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XM_011538082.2:c.4950A>C
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XP_011536384.1:p.Gly1650=
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XM_017019090.1:c.4977A>C
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XP_016874579.1:p.Gly1659=
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NM_015335.5:c.4980A>C
MANE Select
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NP_056150.1:p.Gly1660=
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