ENST00000282541.10:c.247G=
MANE Select
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ENSP00000282541.6:p.Glu83=
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ENST00000282541.9:c.247G=
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ENSP00000282541.5:p.Glu83=
|
|
ENST00000425459.5:c.226-1620G=
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ENSP00000408770.1:n.226-1620G=
|
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ENST00000428684.1:c.69G=
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ENSP00000392199.1:p.Ala23=
|
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ENST00000429432.5:c.130G=
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ENSP00000393861.1:p.Glu44=
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ENST00000431009.1:c.130G=
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ENSP00000416518.1:p.Glu44=
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NM_015141.3:c.247G= , LRG_419t1:c.247G=
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NP_055956.1:p.Glu83=
|
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XM_005264983.2:c.247G=
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XP_005265040.1:p.Glu83=
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XM_006713068.2:c.226-1620G=
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XP_006713131.1:n.226-1620G=
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NM_015141.4:c.247G=
MANE Select
|
NP_055956.1:p.Glu83=
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