ENST00000480188.2:n.1378A>G
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|
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ENST00000696279.1:c.4664A>G
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|
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ENST00000696280.1:n.4433A>G
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|
|
ENST00000696281.1:c.4362A>G
|
ENSP00000512521.1:p.Gln1454=
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ENST00000697921.1:n.3222A>G
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|
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ENST00000697922.1:c.*4334A>G
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ENSP00000513478.1:n.*4334A>G
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ENST00000697923.1:n.4789A>G
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|
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ENST00000223642.3:c.4344A>G
MANE Select
|
ENSP00000223642.1:p.Gln1448=
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ENST00000223642.2:c.4344A>G
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ENSP00000223642.1:p.Gln1448=
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|
NM_001735.2:c.4344A>G , LRG_28t1:c.4344A>G
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NP_001726.2:p.Gln1448=
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XM_011518980.1:c.4359A>G
|
XP_011517282.1:p.Gln1453=
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NM_001317163.1:c.4362A>G
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NP_001304092.1:p.Gln1454=
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NM_001317163.2:c.4362A>G
|
NP_001304092.1:p.Gln1454=
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|
NM_001735.3:c.4344A>G
MANE Select
|
NP_001726.2:p.Gln1448=
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