ENST00000480188.2:n.1427A>G
|
|
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ENST00000696279.1:c.4713A>G
|
|
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ENST00000696280.1:n.4482A>G
|
|
|
ENST00000696281.1:c.4411A>G
|
ENSP00000512521.1:p.Asn1471Asp
|
|
ENST00000697921.1:n.3271A>G
|
|
|
ENST00000697922.1:c.*4383A>G
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ENSP00000513478.1:n.*4383A>G
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|
ENST00000697923.1:n.4838A>G
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|
|
ENST00000223642.3:c.4393A>G
MANE Select
|
ENSP00000223642.1:p.Asn1465Asp
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|
ENST00000223642.2:c.4393A>G
|
ENSP00000223642.1:p.Asn1465Asp
|
|
NM_001735.2:c.4393A>G , LRG_28t1:c.4393A>G
|
NP_001726.2:p.Asn1465Asp
|
|
XM_011518980.1:c.4408A>G
|
XP_011517282.1:p.Asn1470Asp
|
|
NM_001317163.1:c.4411A>G
|
NP_001304092.1:p.Asn1471Asp
|
|
NM_001317163.2:c.4411A>G
|
NP_001304092.1:p.Asn1471Asp
|
|
NM_001735.3:c.4393A>G
MANE Select
|
NP_001726.2:p.Asn1465Asp
|
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