ENST00000328300.11:c.4911A>C
MANE Select
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ENSP00000331902.7:p.Glu1637Asp
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ENST00000361603.7:c.4893A>C
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ENSP00000354505.2:p.Glu1631Asp
|
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ENST00000510690.2:n.1405A>C
|
|
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ENST00000644079.1:n.1742A>C
|
|
|
ENST00000328300.10:c.4911A>C
|
ENSP00000331902.6:p.Glu1637Asp
|
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ENST00000361603.6:c.4893A>C
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ENSP00000354505.2:p.Glu1631Asp
|
|
ENST00000504541.1:c.219+435A>C
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ENSP00000424845.1:n.219+435A>C
|
|
ENST00000515658.1:c.325-941A>C
|
|
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NM_000495.4:c.4893A>C
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NP_000486.1:p.Glu1631Asp
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NM_033380.2:c.4911A>C
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NP_203699.1:p.Glu1637Asp
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XM_005262070.2:c.4902A>C
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XP_005262127.1:p.Glu1634Asp
|
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XM_006724616.2:c.4911A>C
|
XP_006724679.1:p.Glu1637Asp
|
|
XM_011530849.1:c.4587A>C
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XP_011529151.1:p.Glu1529Asp
|
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XM_011530851.1:c.2484A>C
|
XP_011529153.1:p.Glu828Asp
|
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XM_011530849.2:c.4926A>C
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XP_011529151.2:p.Glu1642Asp
|
|
XM_017029259.2:c.4917A>C
|
XP_016884748.1:p.Glu1639Asp
|
|
XM_017029260.1:c.4908A>C
|
XP_016884749.1:p.Glu1636Asp
|
|
XM_017029263.2:c.3246A>C
|
XP_016884752.1:p.Glu1082Asp
|
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NM_000495.5:c.4893A>C
|
NP_000486.1:p.Glu1631Asp
|
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NM_033380.3:c.4911A>C
MANE Select
|
NP_203699.1:p.Glu1637Asp
|
|