ENST00000585465.3:c.*2819G=
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ENSP00000490268.2:n.*2819G=
|
|
ENST00000585748.3:c.846G=
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ENSP00000477641.2:p.Ala282=
|
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ENST00000585851.2:c.1044G=
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ENSP00000467912.2:p.Ala348=
|
|
ENST00000326873.12:c.1218G=
MANE Select
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ENSP00000324856.6:p.Ala406=
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ENST00000326873.11:c.1218G=
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ENSP00000324856.6:p.Ala406=
|
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ENST00000585465.2:n.2951G=
|
|
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ENST00000586243.5:c.1218G=
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ENSP00000467240.2:p.Ala406=
|
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ENST00000589152.5:n.1916G=
|
|
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NM_000455.4:c.1218G= , LRG_319t1:c.1218G=
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NP_000446.1:p.Ala406=
|
|
XM_005259617.1:c.1213G=
|
XP_005259674.1:p.Gly405=
|
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XM_011528209.1:c.991G=
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XP_011526511.1:p.Gly331=
|
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XM_005259617.3:c.1213G=
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XP_005259674.1:p.Gly405=
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XM_011528209.2:c.991G=
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XP_011526511.1:p.Gly331=
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XR_001753738.2:n.2024G=
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|
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XR_001753740.2:n.1994G=
|
|
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NM_000455.5:c.1218G=
MANE Select
|
NP_000446.1:p.Ala406=
|
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