ENST00000356126.8:c.326G>T
MANE Select
|
ENSP00000348442.3:p.Cys109Phe
|
|
ENST00000356126.7:c.326G>T
|
ENSP00000348442.3:p.Cys109Phe
|
|
ENST00000357146.4:c.266G>T
|
ENSP00000349667.4:p.Cys89Phe
|
|
ENST00000579365.5:c.*376G>T
|
ENSP00000463017.1:n.*376G>T
|
|
ENST00000581618.1:n.563G>T
|
|
|
ENST00000584008.5:c.*481G>T
|
ENSP00000462525.1:n.*481G>T
|
|
ENST00000584289.5:n.375G>T
|
|
|
NM_001316341.1:c.149G>T
|
NP_001303270.1:p.Cys50Phe
|
|
NM_002816.3:c.326G>T
|
NP_002807.1:p.Cys109Phe
|
|
NM_002816.4:c.326G>T
|
NP_002807.1:p.Cys109Phe
|
|
NM_174871.2:c.266G>T
|
NP_777360.1:p.Cys89Phe
|
|
NM_174871.3:c.266G>T
|
NP_777360.1:p.Cys89Phe
|
|
XM_011525048.1:c.149G>T
|
XP_011523350.1:p.Cys50Phe
|
|
XM_011525049.1:c.149G>T
|
XP_011523351.1:p.Cys50Phe
|
|
XM_011525050.1:c.326G>T
|
XP_011523352.1:p.Cys109Phe
|
|
XM_024450842.1:c.413G>T
|
XP_024306610.1:p.Cys138Phe
|
|
XM_024450843.1:c.149G>T
|
XP_024306611.1:p.Cys50Phe
|
|
XR_001752571.2:n.405G>T
|
|
|
NM_002816.5:c.326G>T
MANE Select
|
NP_002807.1:p.Cys109Phe
|
|
NM_001316341.2:c.149G>T
|
NP_001303270.1:p.Cys50Phe
|
|
NM_174871.4:c.266G>T
|
NP_777360.1:p.Cys89Phe
|
|