ENST00000355832.10:c.3575A>T
MANE Select
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ENSP00000348089.5:p.Glu1192Val
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ENST00000679552.1:n.646A>T
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|
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ENST00000679871.1:n.721A>T
|
|
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ENST00000679974.1:n.624A>T
|
|
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ENST00000681632.1:n.4978A>T
|
|
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ENST00000681659.1:c.3416A>T
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ENSP00000505631.1:p.Glu1139Val
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ENST00000355832.9:c.3575A>T
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ENSP00000348089.5:p.Glu1192Val
|
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ENST00000623073.3:c.*1871A>T
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ENSP00000485650.1:n.*1871A>T
|
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ENST00000623115.3:c.1685A>T
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ENSP00000485321.1:p.Glu562Val
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ENST00000624341.3:c.1407A>T
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NM_000124.3:c.3575A>T
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NP_000115.1:p.Glu1192Val
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XR_945953.1:n.243-1180T>A
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|
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NM_001346440.1:c.3575A>T
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NP_001333369.1:p.Glu1192Val
|
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NM_000124.4:c.3575A>T
MANE Select
|
NP_000115.1:p.Glu1192Val
|
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NM_001346440.2:c.3575A>T
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NP_001333369.1:p.Glu1192Val
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