ENST00000480188.2:n.1365A>T
|
|
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ENST00000696279.1:c.4651A>T
|
|
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ENST00000696280.1:n.4420A>T
|
|
|
ENST00000696281.1:c.4349A>T
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ENSP00000512521.1:p.Glu1450Val
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|
ENST00000697921.1:n.3209A>T
|
|
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ENST00000697922.1:c.*4321A>T
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ENSP00000513478.1:n.*4321A>T
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|
ENST00000697923.1:n.4776A>T
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|
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ENST00000223642.3:c.4331A>T
MANE Select
|
ENSP00000223642.1:p.Glu1444Val
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|
ENST00000223642.2:c.4331A>T
|
ENSP00000223642.1:p.Glu1444Val
|
|
NM_001735.2:c.4331A>T , LRG_28t1:c.4331A>T
|
NP_001726.2:p.Glu1444Val
|
|
XM_011518980.1:c.4346A>T
|
XP_011517282.1:p.Glu1449Val
|
|
NM_001317163.1:c.4349A>T
|
NP_001304092.1:p.Glu1450Val
|
|
NM_001317163.2:c.4349A>T
|
NP_001304092.1:p.Glu1450Val
|
|
NM_001735.3:c.4331A>T
MANE Select
|
NP_001726.2:p.Glu1444Val
|
|