ENST00000252029.8:c.377G>C
MANE Select
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ENSP00000252029.3:p.Ser126Thr
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ENST00000395680.6:c.377G>C
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ENSP00000379037.1:p.Ser126Thr
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ENST00000395681.6:c.377G>C
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ENSP00000379038.1:p.Ser126Thr
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ENST00000650719.1:c.377G>C
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ENSP00000498276.1:p.Ser126Thr
|
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ENST00000651095.1:n.516G>C
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|
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ENST00000651196.1:c.377G>C
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ENSP00000499096.1:p.Ser126Thr
|
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ENST00000651401.1:c.-1+728G>C
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ENSP00000499115.1:n.-1+728G>C
|
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ENST00000651906.1:n.496G>C
|
|
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ENST00000652237.1:n.653G>C
|
|
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ENST00000652352.1:c.125G>C
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ENSP00000498579.1:p.Ser42Thr
|
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ENST00000252029.7:c.377G>C
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ENSP00000252029.3:p.Ser126Thr
|
|
ENST00000395678.7:c.377G>C
|
ENSP00000379036.3:p.Ser126Thr
|
|
ENST00000395680.5:c.377G>C
|
ENSP00000379037.1:p.Ser126Thr
|
|
ENST00000395681.5:c.377G>C
|
ENSP00000379038.1:p.Ser126Thr
|
|
ENST00000425169.1:c.377G>C
|
ENSP00000395875.1:p.Ser126Thr
|
|
ENST00000476284.1:n.502G>C
|
|
|
ENST00000487162.1:n.665G>C
|
|
|
ENST00000487577.5:n.664G>C
|
|
|
NM_001113755.2:c.377G>C
|
NP_001107227.1:p.Ser126Thr
|
|
NM_001113756.2:c.377G>C
|
NP_001107228.1:p.Ser126Thr
|
|
NM_001257988.1:c.377G>C , LRG_727t1:c.377G>C
|
NP_001244917.1:p.Ser126Thr
|
|
NM_001257989.1:c.377G>C , LRG_727t2:c.377G>C
|
NP_001244918.1:p.Ser126Thr
|
|
NM_001953.4:c.377G>C
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NP_001944.1:p.Ser126Thr
|
|
NM_001113755.3:c.377G>C
|
NP_001107227.1:p.Ser126Thr
|
|
NM_001113756.3:c.377G>C
|
NP_001107228.1:p.Ser126Thr
|
|
NM_001953.5:c.377G>C
MANE Select
|
NP_001944.1:p.Ser126Thr
|
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