ENST00000328300.11:c.4852C>G
MANE Select
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ENSP00000331902.7:p.Gln1618Glu
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ENST00000361603.7:c.4834C>G
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ENSP00000354505.2:p.Gln1612Glu
|
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ENST00000510690.2:n.1346C>G
|
|
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ENST00000644079.1:n.1683C>G
|
|
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ENST00000328300.10:c.4852C>G
|
ENSP00000331902.6:p.Gln1618Glu
|
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ENST00000361603.6:c.4834C>G
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ENSP00000354505.2:p.Gln1612Glu
|
|
ENST00000504541.1:c.219+376C>G
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ENSP00000424845.1:n.219+376C>G
|
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ENST00000515658.1:c.325-1000C>G
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|
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NM_000495.4:c.4834C>G
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NP_000486.1:p.Gln1612Glu
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NM_033380.2:c.4852C>G
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NP_203699.1:p.Gln1618Glu
|
|
XM_005262070.2:c.4843C>G
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XP_005262127.1:p.Gln1615Glu
|
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XM_006724616.2:c.4852C>G
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XP_006724679.1:p.Gln1618Glu
|
|
XM_011530849.1:c.4528C>G
|
XP_011529151.1:p.Gln1510Glu
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XM_011530851.1:c.2425C>G
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XP_011529153.1:p.Gln809Glu
|
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XM_011530849.2:c.4867C>G
|
XP_011529151.2:p.Gln1623Glu
|
|
XM_017029259.2:c.4858C>G
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XP_016884748.1:p.Gln1620Glu
|
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XM_017029260.1:c.4849C>G
|
XP_016884749.1:p.Gln1617Glu
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XM_017029263.2:c.3187C>G
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XP_016884752.1:p.Gln1063Glu
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NM_000495.5:c.4834C>G
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NP_000486.1:p.Gln1612Glu
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NM_033380.3:c.4852C>G
MANE Select
|
NP_203699.1:p.Gln1618Glu
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