ENST00000328300.11:c.4900C>G
MANE Select
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ENSP00000331902.7:p.Pro1634Ala
|
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ENST00000361603.7:c.4882C>G
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ENSP00000354505.2:p.Pro1628Ala
|
|
ENST00000510690.2:n.1394C>G
|
|
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ENST00000644079.1:n.1731C>G
|
|
|
ENST00000328300.10:c.4900C>G
|
ENSP00000331902.6:p.Pro1634Ala
|
|
ENST00000361603.6:c.4882C>G
|
ENSP00000354505.2:p.Pro1628Ala
|
|
ENST00000504541.1:c.219+424C>G
|
ENSP00000424845.1:n.219+424C>G
|
|
ENST00000515658.1:c.325-952C>G
|
|
|
NM_000495.4:c.4882C>G
|
NP_000486.1:p.Pro1628Ala
|
|
NM_033380.2:c.4900C>G
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NP_203699.1:p.Pro1634Ala
|
|
XM_005262070.2:c.4891C>G
|
XP_005262127.1:p.Pro1631Ala
|
|
XM_006724616.2:c.4900C>G
|
XP_006724679.1:p.Pro1634Ala
|
|
XM_011530849.1:c.4576C>G
|
XP_011529151.1:p.Pro1526Ala
|
|
XM_011530851.1:c.2473C>G
|
XP_011529153.1:p.Pro825Ala
|
|
XM_011530849.2:c.4915C>G
|
XP_011529151.2:p.Pro1639Ala
|
|
XM_017029259.2:c.4906C>G
|
XP_016884748.1:p.Pro1636Ala
|
|
XM_017029260.1:c.4897C>G
|
XP_016884749.1:p.Pro1633Ala
|
|
XM_017029263.2:c.3235C>G
|
XP_016884752.1:p.Pro1079Ala
|
|
NM_000495.5:c.4882C>G
|
NP_000486.1:p.Pro1628Ala
|
|
NM_033380.3:c.4900C>G
MANE Select
|
NP_203699.1:p.Pro1634Ala
|
|