ENST00000328300.11:c.4920G>T
MANE Select
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ENSP00000331902.7:p.Gly1640=
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ENST00000361603.7:c.4902G>T
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ENSP00000354505.2:p.Gly1634=
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ENST00000510690.2:n.1414G>T
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ENST00000644079.1:n.1751G>T
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ENST00000328300.10:c.4920G>T
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ENSP00000331902.6:p.Gly1640=
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ENST00000361603.6:c.4902G>T
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ENSP00000354505.2:p.Gly1634=
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ENST00000504541.1:c.219+444G>T
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ENSP00000424845.1:n.219+444G>T
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ENST00000515658.1:c.325-932G>T
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NM_000495.4:c.4902G>T
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NP_000486.1:p.Gly1634=
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NM_033380.2:c.4920G>T
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NP_203699.1:p.Gly1640=
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XM_005262070.2:c.4911G>T
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XP_005262127.1:p.Gly1637=
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XM_006724616.2:c.4920G>T
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XP_006724679.1:p.Gly1640=
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XM_011530849.1:c.4596G>T
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XP_011529151.1:p.Gly1532=
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XM_011530851.1:c.2493G>T
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XP_011529153.1:p.Gly831=
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XM_011530849.2:c.4935G>T
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XP_011529151.2:p.Gly1645=
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XM_017029259.2:c.4926G>T
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XP_016884748.1:p.Gly1642=
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XM_017029260.1:c.4917G>T
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XP_016884749.1:p.Gly1639=
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XM_017029263.2:c.3255G>T
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XP_016884752.1:p.Gly1085=
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NM_000495.5:c.4902G>T
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NP_000486.1:p.Gly1634=
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NM_033380.3:c.4920G>T
MANE Select
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NP_203699.1:p.Gly1640=
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