ENST00000373247.7:c.1659G=
MANE Select
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ENSP00000362344.2:p.Gly553=
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|
ENST00000373225.7:c.1509G=
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ENSP00000362322.3:p.Gly503=
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|
ENST00000373247.6:c.1659G=
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ENSP00000362344.2:p.Gly553=
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|
ENST00000393706.6:c.1581G=
|
ENSP00000377309.2:p.Gly527=
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|
ENST00000460181.5:n.1647G=
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|
|
ENST00000467826.5:n.709+176G=
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|
|
ENST00000475270.1:n.485G=
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|
|
ENST00000630236.2:c.*383G=
|
ENSP00000486766.1:n.*383G=
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|
NM_001018078.2:c.1509G=
|
NP_001018088.1:p.Gly503=
|
|
NM_001288803.1:c.1581G=
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NP_001275732.1:p.Gly527=
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|
NM_004957.5:c.1659G=
|
NP_004948.4:p.Gly553=
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|
NR_110170.1:n.1707G=
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|
|
XM_005251864.2:c.1483+176G=
|
XP_005251921.1:n.1483+176G=
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|
XM_011518437.1:c.1509G=
|
XP_011516739.1:p.Gly503=
|
|
XM_011518438.1:c.1509G=
|
XP_011516740.1:p.Gly503=
|
|
XM_011518439.1:c.816G=
|
XP_011516741.1:p.Gly272=
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|
XR_242581.2:n.1556G=
|
|
|
XR_242582.2:n.1380+176G=
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|
|
XM_005251864.4:c.1483+176G=
|
XP_005251921.1:n.1483+176G=
|
|
XM_011518439.2:c.816G=
|
XP_011516741.1:p.Gly272=
|
|
XM_017014565.2:c.1333+176G=
|
XP_016870054.1:n.1333+176G=
|
|
XM_017014566.1:c.816G=
|
XP_016870055.1:p.Gly272=
|
|
XR_242581.4:n.1554G=
|
|
|
XR_242582.4:n.1378+176G=
|
|
|
NM_004957.6:c.1659G=
MANE Select
|
NP_004948.4:p.Gly553=
|
|