ENST00000480188.2:n.1426G>A
|
|
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ENST00000696279.1:c.4712G>A
|
|
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ENST00000696280.1:n.4481G>A
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|
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ENST00000696281.1:c.4410G>A
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ENSP00000512521.1:p.Leu1470=
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ENST00000697921.1:n.3270G>A
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|
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ENST00000697922.1:c.*4382G>A
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ENSP00000513478.1:n.*4382G>A
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|
ENST00000697923.1:n.4837G>A
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|
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ENST00000223642.3:c.4392G>A
MANE Select
|
ENSP00000223642.1:p.Leu1464=
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ENST00000223642.2:c.4392G>A
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ENSP00000223642.1:p.Leu1464=
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NM_001735.2:c.4392G>A , LRG_28t1:c.4392G>A
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NP_001726.2:p.Leu1464=
|
|
XM_011518980.1:c.4407G>A
|
XP_011517282.1:p.Leu1469=
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|
NM_001317163.1:c.4410G>A
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NP_001304092.1:p.Leu1470=
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|
NM_001317163.2:c.4410G>A
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NP_001304092.1:p.Leu1470=
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|
NM_001735.3:c.4392G>A
MANE Select
|
NP_001726.2:p.Leu1464=
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