ENST00000480188.2:n.1456T>A
|
|
|
ENST00000696279.1:c.4742T>A
|
|
|
ENST00000696280.1:n.4511T>A
|
|
|
ENST00000696281.1:c.4440T>A
|
ENSP00000512521.1:p.Cys1480Ter
|
|
ENST00000697921.1:n.3300T>A
|
|
|
ENST00000697922.1:c.*4412T>A
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ENSP00000513478.1:n.*4412T>A
|
|
ENST00000697923.1:n.4867T>A
|
|
|
ENST00000223642.3:c.4422T>A
MANE Select
|
ENSP00000223642.1:p.Cys1474Ter
|
|
ENST00000223642.2:c.4422T>A
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ENSP00000223642.1:p.Cys1474Ter
|
|
NM_001735.2:c.4422T>A , LRG_28t1:c.4422T>A
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NP_001726.2:p.Cys1474Ter
|
|
XM_011518980.1:c.4437T>A
|
XP_011517282.1:p.Cys1479Ter
|
|
NM_001317163.1:c.4440T>A
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NP_001304092.1:p.Cys1480Ter
|
|
NM_001317163.2:c.4440T>A
|
NP_001304092.1:p.Cys1480Ter
|
|
NM_001735.3:c.4422T>A
MANE Select
|
NP_001726.2:p.Cys1474Ter
|
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