ENST00000330062.8:c.554T>A
MANE Select
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ENSP00000331897.4:p.Val185Glu
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ENST00000330062.7:c.554T>A
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ENSP00000331897.3:p.Val185Glu
|
|
ENST00000540499.2:c.398T>A
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ENSP00000446147.2:p.Val133Glu
|
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ENST00000559482.5:c.227T>A
|
ENSP00000453016.1:p.Val76Glu
|
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ENST00000560061.1:c.*179T>A
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ENSP00000453254.1:n.*179T>A
|
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NM_001289910.1:c.398T>A , LRG_611t1:c.398T>A
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NP_001276839.1:p.Val133Glu
|
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NM_001290114.1:c.164T>A
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NP_001277043.1:p.Val55Glu
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NM_002168.3:c.554T>A , LRG_611t2:c.554T>A
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NP_002159.2:p.Val185Glu
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NM_001290114.2:c.164T>A
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NP_001277043.1:p.Val55Glu
|
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NM_002168.4:c.554T>A
MANE Select
|
NP_002159.2:p.Val185Glu
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