ENST00000696217.1:n.529G>A
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|
|
ENST00000219150.10:c.448G>A
MANE Select
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ENSP00000219150.6:p.Ala150Thr
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|
ENST00000219150.9:c.448G>A
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ENSP00000219150.5:p.Ala150Thr
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|
ENST00000561815.5:c.556G>A
|
ENSP00000456756.1:p.Ala186Thr
|
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ENST00000563778.5:c.448G>A
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ENSP00000456266.1:p.Ala150Thr
|
|
ENST00000564768.1:n.261G>A
|
|
|
ENST00000565497.5:c.448G>A
|
ENSP00000456457.1:p.Ala150Thr
|
|
ENST00000567034.5:n.916G>A
|
|
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ENST00000568763.1:n.1760G>A
|
|
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ENST00000568982.5:n.566G>A
|
|
|
ENST00000569469.1:n.432-97G>A
|
|
|
ENST00000569970.1:c.448G>A
|
ENSP00000457509.1:p.Ala150Thr
|
|
ENST00000570045.5:c.448G>A
|
ENSP00000455552.1:p.Ala150Thr
|
|
ENST00000570244.5:c.325G>A
|
ENSP00000457332.1:p.Ala109Thr
|
|
NM_001193333.2:c.448G>A
|
NP_001180262.1:p.Ala150Thr
|
|
NM_007074.3:c.448G>A
|
NP_009005.1:p.Ala150Thr
|
|
XM_011545714.1:c.448G>A
|
XP_011544016.1:p.Ala150Thr
|
|
XM_011545714.2:c.448G>A
|
XP_011544016.1:p.Ala150Thr
|
|
XM_017022885.2:c.448G>A
|
XP_016878374.1:p.Ala150Thr
|
|
XM_017022886.1:c.448G>A
|
XP_016878375.1:p.Ala150Thr
|
|
NM_007074.4:c.448G>A
MANE Select
|
NP_009005.1:p.Ala150Thr
|
|
NM_001193333.3:c.448G>A
|
NP_001180262.1:p.Ala150Thr
|
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