ENST00000480188.2:n.1483T>G
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|
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ENST00000696279.1:c.4769T>G
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|
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ENST00000696280.1:n.4538T>G
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|
|
ENST00000696281.1:c.4467T>G
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ENSP00000512521.1:p.Phe1489Leu
|
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ENST00000697921.1:n.3327T>G
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|
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ENST00000697922.1:c.*4439T>G
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ENSP00000513478.1:n.*4439T>G
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ENST00000697923.1:n.4894T>G
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|
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ENST00000223642.3:c.4449T>G
MANE Select
|
ENSP00000223642.1:p.Phe1483Leu
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ENST00000223642.2:c.4449T>G
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ENSP00000223642.1:p.Phe1483Leu
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NM_001735.2:c.4449T>G , LRG_28t1:c.4449T>G
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NP_001726.2:p.Phe1483Leu
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XM_011518980.1:c.4464T>G
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XP_011517282.1:p.Phe1488Leu
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NM_001317163.1:c.4467T>G
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NP_001304092.1:p.Phe1489Leu
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NM_001317163.2:c.4467T>G
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NP_001304092.1:p.Phe1489Leu
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NM_001735.3:c.4449T>G
MANE Select
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NP_001726.2:p.Phe1483Leu
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