ENST00000480188.2:n.1476A>T
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|
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ENST00000696279.1:c.4762A>T
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|
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ENST00000696280.1:n.4531A>T
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|
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ENST00000696281.1:c.4460A>T
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ENSP00000512521.1:p.Glu1487Val
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ENST00000697921.1:n.3320A>T
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|
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ENST00000697922.1:c.*4432A>T
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ENSP00000513478.1:n.*4432A>T
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ENST00000697923.1:n.4887A>T
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|
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ENST00000223642.3:c.4442A>T
MANE Select
|
ENSP00000223642.1:p.Glu1481Val
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ENST00000223642.2:c.4442A>T
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ENSP00000223642.1:p.Glu1481Val
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|
NM_001735.2:c.4442A>T , LRG_28t1:c.4442A>T
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NP_001726.2:p.Glu1481Val
|
|
XM_011518980.1:c.4457A>T
|
XP_011517282.1:p.Glu1486Val
|
|
NM_001317163.1:c.4460A>T
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NP_001304092.1:p.Glu1487Val
|
|
NM_001317163.2:c.4460A>T
|
NP_001304092.1:p.Glu1487Val
|
|
NM_001735.3:c.4442A>T
MANE Select
|
NP_001726.2:p.Glu1481Val
|
|