ENST00000350051.8:c.419C>A
MANE Select
|
ENSP00000324180.4:p.Ala140Asp
|
|
ENST00000301633.8:c.488C>A
|
ENSP00000301633.3:p.Ala163Asp
|
|
ENST00000350051.7:c.419C>A
|
ENSP00000324180.4:p.Ala140Asp
|
|
ENST00000374948.6:c.301C>A
|
ENSP00000364086.1:p.Pro101Thr
|
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ENST00000589892.1:n.435C>A
|
|
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ENST00000590925.6:c.*221C>A
|
ENSP00000467336.1:n.*221C>A
|
|
NM_001012270.1:c.301C>A
|
NP_001012270.1:p.Pro101Thr
|
|
NM_001012271.1:c.488C>A
|
NP_001012271.1:p.Ala163Asp
|
|
NM_001168.2:c.419C>A
|
NP_001159.2:p.Ala140Asp
|
|
XR_243654.3:n.621C>A
|
|
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XR_934452.1:n.690C>A
|
|
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XR_243654.5:n.621C>A
|
|
|
XR_934452.3:n.690C>A
|
|
|
NM_001168.3:c.419C>A
MANE Select
|
NP_001159.2:p.Ala140Asp
|
|
NM_001012270.2:c.301C>A
|
NP_001012270.1:p.Pro101Thr
|
|
NM_001012271.2:c.488C>A
|
NP_001012271.1:p.Ala163Asp
|
|