ENST00000398603.6:c.427G>A
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ENSP00000381604.1:p.Ala143Thr
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ENST00000398606.10:c.535G>A
MANE Select
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ENSP00000381607.3:p.Ala179Thr
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ENST00000646888.1:c.*251G>A
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ENSP00000494477.1:n.*251G>A
|
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ENST00000398603.5:c.427G>A
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ENSP00000381604.1:p.Ala143Thr
|
|
ENST00000398606.7:c.535G>A
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ENSP00000381607.3:p.Ala179Thr
|
|
ENST00000467591.1:n.646G>A
|
|
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ENST00000494593.1:n.1507G>A
|
|
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ENST00000498765.5:c.598G>A
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|
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NM_000852.3:c.535G>A , LRG_723t1:c.535G>A
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NP_000843.1:p.Ala179Thr
|
|
NM_000852.4:c.535G>A
MANE Select
|
NP_000843.1:p.Ala179Thr
|
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