ENST00000356392.9:c.863A>T
MANE Select
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ENSP00000348757.3:p.Glu288Val
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|
ENST00000356392.8:c.863A>T
|
ENSP00000348757.3:p.Glu288Val
|
|
ENST00000586836.5:c.290A>T
|
ENSP00000467429.1:p.Glu97Val
|
|
ENST00000591179.5:c.683A>T
|
ENSP00000466800.1:p.Glu228Val
|
|
ENST00000591345.5:c.*782A>T
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ENSP00000467313.1:n.*782A>T
|
|
NM_001302453.1:c.701A>T
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NP_001289382.1:p.Glu234Val
|
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NM_001302454.1:c.683A>T
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NP_001289383.1:p.Glu228Val
|
|
NM_145045.4:c.863A>T
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NP_659482.3:p.Glu288Val
|
|
XM_017026241.1:c.863A>T
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XP_016881730.1:p.Glu288Val
|
|
NM_145045.5:c.863A>T
MANE Select
|
NP_659482.3:p.Glu288Val
|
|
NM_001302454.2:c.683A>T
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NP_001289383.1:p.Glu228Val
|
|