ENST00000272602.7:c.1573G=
MANE Select
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ENSP00000272602.2:p.Gly525=
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ENST00000272602.6:c.1573G=
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ENSP00000272602.2:p.Gly525=
|
|
ENST00000393504.5:c.1573G=
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ENSP00000377140.1:p.Gly525=
|
|
ENST00000409937.1:c.1585G=
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ENSP00000386761.1:p.Gly529=
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|
ENST00000436404.6:c.1519G=
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ENSP00000410070.2:p.Gly507=
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NM_001079878.1:c.1519G=
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NP_001073347.1:p.Gly507=
|
|
NM_001298.2:c.1573G=
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NP_001289.1:p.Gly525=
|
|
XM_006712243.2:c.1684G=
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XP_006712306.1:p.Gly562=
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|
XM_011510554.1:c.1738G=
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XP_011508856.1:p.Gly580=
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|
XM_011510554.2:c.1738G=
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XP_011508856.1:p.Gly580=
|
|
NM_001079878.2:c.1519G=
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NP_001073347.1:p.Gly507=
|
|
NM_001298.3:c.1573G=
MANE Select
|
NP_001289.1:p.Gly525=
|
|