ENST00000480188.2:n.1478C>T
|
|
|
ENST00000696279.1:c.4764C>T
|
|
|
ENST00000696280.1:n.4533C>T
|
|
|
ENST00000696281.1:c.4462C>T
|
ENSP00000512521.1:p.Leu1488Phe
|
|
ENST00000697921.1:n.3322C>T
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|
|
ENST00000697922.1:c.*4434C>T
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ENSP00000513478.1:n.*4434C>T
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|
ENST00000697923.1:n.4889C>T
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|
|
ENST00000223642.3:c.4444C>T
MANE Select
|
ENSP00000223642.1:p.Leu1482Phe
|
|
ENST00000223642.2:c.4444C>T
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ENSP00000223642.1:p.Leu1482Phe
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|
NM_001735.2:c.4444C>T , LRG_28t1:c.4444C>T
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NP_001726.2:p.Leu1482Phe
|
|
XM_011518980.1:c.4459C>T
|
XP_011517282.1:p.Leu1487Phe
|
|
NM_001317163.1:c.4462C>T
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NP_001304092.1:p.Leu1488Phe
|
|
NM_001317163.2:c.4462C>T
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NP_001304092.1:p.Leu1488Phe
|
|
NM_001735.3:c.4444C>T
MANE Select
|
NP_001726.2:p.Leu1482Phe
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