ENST00000272602.7:c.1683G=
MANE Select
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ENSP00000272602.2:p.Gly561=
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ENST00000272602.6:c.1683G=
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ENSP00000272602.2:p.Gly561=
|
|
ENST00000393504.5:c.1683G=
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ENSP00000377140.1:p.Gly561=
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|
ENST00000409937.1:c.1695G=
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ENSP00000386761.1:p.Gly565=
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ENST00000436404.6:c.1629G=
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ENSP00000410070.2:p.Gly543=
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NM_001079878.1:c.1629G=
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NP_001073347.1:p.Gly543=
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|
NM_001298.2:c.1683G=
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NP_001289.1:p.Gly561=
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XM_006712243.2:c.1794G=
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XP_006712306.1:p.Gly598=
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XM_011510554.1:c.1848G=
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XP_011508856.1:p.Gly616=
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|
XM_011510554.2:c.1848G=
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XP_011508856.1:p.Gly616=
|
|
NM_001079878.2:c.1629G=
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NP_001073347.1:p.Gly543=
|
|
NM_001298.3:c.1683G=
MANE Select
|
NP_001289.1:p.Gly561=
|
|