ENST00000398603.6:c.409G>A
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ENSP00000381604.1:p.Ala137Thr
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ENST00000398606.10:c.517G>A
MANE Select
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ENSP00000381607.3:p.Ala173Thr
|
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ENST00000646888.1:c.*233G>A
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ENSP00000494477.1:n.*233G>A
|
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ENST00000398603.5:c.409G>A
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ENSP00000381604.1:p.Ala137Thr
|
|
ENST00000398606.7:c.517G>A
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ENSP00000381607.3:p.Ala173Thr
|
|
ENST00000467591.1:n.628G>A
|
|
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ENST00000494593.1:n.1489G>A
|
|
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ENST00000498765.5:c.580G>A
|
|
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NM_000852.3:c.517G>A , LRG_723t1:c.517G>A
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NP_000843.1:p.Ala173Thr
|
|
NM_000852.4:c.517G>A
MANE Select
|
NP_000843.1:p.Ala173Thr
|
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