ENST00000355832.10:c.3876T>A
MANE Select
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ENSP00000348089.5:p.Asp1292Glu
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ENST00000679552.1:n.947T>A
|
|
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ENST00000679871.1:n.1022T>A
|
|
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ENST00000679974.1:n.925T>A
|
|
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ENST00000681632.1:n.5279T>A
|
|
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ENST00000681659.1:c.3717T>A
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ENSP00000505631.1:p.Asp1239Glu
|
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ENST00000355832.9:c.3876T>A
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ENSP00000348089.5:p.Asp1292Glu
|
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ENST00000465653.1:n.198T>A
|
|
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ENST00000623073.3:c.*2172T>A
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ENSP00000485650.1:n.*2172T>A
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ENST00000623115.3:c.1986T>A
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ENSP00000485321.1:p.Asp662Glu
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ENST00000624341.3:c.1708T>A
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|
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NM_000124.3:c.3876T>A
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NP_000115.1:p.Asp1292Glu
|
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XR_945953.1:n.243-10106A>T
|
|
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NM_001346440.1:c.3876T>A
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NP_001333369.1:p.Asp1292Glu
|
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NM_000124.4:c.3876T>A
MANE Select
|
NP_000115.1:p.Asp1292Glu
|
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NM_001346440.2:c.3876T>A
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NP_001333369.1:p.Asp1292Glu
|
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