ENST00000355832.10:c.2941T>G
MANE Select
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ENSP00000348089.5:p.Phe981Val
|
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ENST00000679552.1:n.142-215T>G
|
|
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ENST00000679871.1:n.87T>G
|
|
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ENST00000679974.1:n.120-215T>G
|
|
|
ENST00000681632.1:n.4344T>G
|
|
|
ENST00000681659.1:c.2782T>G
|
ENSP00000505631.1:p.Phe928Val
|
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ENST00000355832.9:c.2941T>G
|
ENSP00000348089.5:p.Phe981Val
|
|
ENST00000623073.3:c.*1237T>G
|
ENSP00000485650.1:n.*1237T>G
|
|
ENST00000623115.3:c.1051T>G
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ENSP00000485321.1:p.Phe351Val
|
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ENST00000624341.3:c.773T>G
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|
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NM_000124.3:c.2941T>G
|
NP_000115.1:p.Phe981Val
|
|
XR_945953.1:n.243-461A>C
|
|
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NM_001346440.1:c.2941T>G
|
NP_001333369.1:p.Phe981Val
|
|
NM_000124.4:c.2941T>G
MANE Select
|
NP_000115.1:p.Phe981Val
|
|
NM_001346440.2:c.2941T>G
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NP_001333369.1:p.Phe981Val
|
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