ENST00000328300.11:c.4884A>C
MANE Select
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ENSP00000331902.7:p.Glu1628Asp
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ENST00000361603.7:c.4866A>C
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ENSP00000354505.2:p.Glu1622Asp
|
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ENST00000510690.2:n.1378A>C
|
|
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ENST00000644079.1:n.1715A>C
|
|
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ENST00000328300.10:c.4884A>C
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ENSP00000331902.6:p.Glu1628Asp
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ENST00000361603.6:c.4866A>C
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ENSP00000354505.2:p.Glu1622Asp
|
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ENST00000504541.1:c.219+408A>C
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ENSP00000424845.1:n.219+408A>C
|
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ENST00000515658.1:c.325-968A>C
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NM_000495.4:c.4866A>C
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NP_000486.1:p.Glu1622Asp
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NM_033380.2:c.4884A>C
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NP_203699.1:p.Glu1628Asp
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XM_005262070.2:c.4875A>C
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XP_005262127.1:p.Glu1625Asp
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XM_006724616.2:c.4884A>C
|
XP_006724679.1:p.Glu1628Asp
|
|
XM_011530849.1:c.4560A>C
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XP_011529151.1:p.Glu1520Asp
|
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XM_011530851.1:c.2457A>C
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XP_011529153.1:p.Glu819Asp
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XM_011530849.2:c.4899A>C
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XP_011529151.2:p.Glu1633Asp
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XM_017029259.2:c.4890A>C
|
XP_016884748.1:p.Glu1630Asp
|
|
XM_017029260.1:c.4881A>C
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XP_016884749.1:p.Glu1627Asp
|
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XM_017029263.2:c.3219A>C
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XP_016884752.1:p.Glu1073Asp
|
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NM_000495.5:c.4866A>C
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NP_000486.1:p.Glu1622Asp
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NM_033380.3:c.4884A>C
MANE Select
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NP_203699.1:p.Glu1628Asp
|
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