ENST00000350051.8:c.401C>A
MANE Select
|
ENSP00000324180.4:p.Ala134Asp
|
|
ENST00000301633.8:c.470C>A
|
ENSP00000301633.3:p.Ala157Asp
|
|
ENST00000350051.7:c.401C>A
|
ENSP00000324180.4:p.Ala134Asp
|
|
ENST00000374948.6:c.283C>A
|
ENSP00000364086.1:p.Pro95Thr
|
|
ENST00000589892.1:n.417C>A
|
|
|
ENST00000590925.6:c.*203C>A
|
ENSP00000467336.1:n.*203C>A
|
|
NM_001012270.1:c.283C>A
|
NP_001012270.1:p.Pro95Thr
|
|
NM_001012271.1:c.470C>A
|
NP_001012271.1:p.Ala157Asp
|
|
NM_001168.2:c.401C>A
|
NP_001159.2:p.Ala134Asp
|
|
XR_243654.3:n.603C>A
|
|
|
XR_934452.1:n.672C>A
|
|
|
XR_243654.5:n.603C>A
|
|
|
XR_934452.3:n.672C>A
|
|
|
NM_001168.3:c.401C>A
MANE Select
|
NP_001159.2:p.Ala134Asp
|
|
NM_001012270.2:c.283C>A
|
NP_001012270.1:p.Pro95Thr
|
|
NM_001012271.2:c.470C>A
|
NP_001012271.1:p.Ala157Asp
|
|