ENST00000309383.6:c.2171C>G
MANE Select
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ENSP00000310649.1:p.Ala724Gly
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ENST00000309383.5:c.2171C>G
|
ENSP00000310649.1:p.Ala724Gly
|
|
ENST00000326848.7:c.1256C>G
|
ENSP00000320853.7:p.Ala419Gly
|
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ENST00000590333.5:c.2219C>G
|
ENSP00000468190.1:p.Ala740Gly
|
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NM_032430.1:c.2171C>G
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NP_115806.1:p.Ala724Gly
|
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XM_005259327.2:c.1901C>G
|
XP_005259384.1:p.Ala634Gly
|
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XM_011527395.1:c.1928C>G
|
XP_011525697.1:p.Ala643Gly
|
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XR_430213.2:n.2154C>G
|
|
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XM_005259327.3:c.1901C>G
|
XP_005259384.1:p.Ala634Gly
|
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XM_011527395.2:c.1643C>G
|
XP_011525697.2:p.Ala548Gly
|
|
XM_024451739.1:c.1946C>G
|
XP_024307507.1:p.Ala649Gly
|
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XR_430213.4:n.2452C>G
|
|
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NM_032430.2:c.2171C>G
MANE Select
|
NP_115806.1:p.Ala724Gly
|
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