ENST00000398603.6:c.448G>A
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ENSP00000381604.1:p.Ala150Thr
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|
ENST00000398606.10:c.556G>A
MANE Select
|
ENSP00000381607.3:p.Ala186Thr
|
|
ENST00000646888.1:c.*272G>A
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ENSP00000494477.1:n.*272G>A
|
|
ENST00000398603.5:c.448G>A
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ENSP00000381604.1:p.Ala150Thr
|
|
ENST00000398606.7:c.556G>A
|
ENSP00000381607.3:p.Ala186Thr
|
|
ENST00000467591.1:n.667G>A
|
|
|
ENST00000494593.1:n.1528G>A
|
|
|
ENST00000498765.5:c.619G>A
|
|
|
NM_000852.3:c.556G>A , LRG_723t1:c.556G>A
|
NP_000843.1:p.Ala186Thr
|
|
NM_000852.4:c.556G>A
MANE Select
|
NP_000843.1:p.Ala186Thr
|
|