ENST00000322048.12:c.684T>A
MANE Select
|
ENSP00000322832.6:p.Pro228=
|
|
ENST00000322048.11:c.684T>A
|
ENSP00000322832.5:p.Pro228=
|
|
ENST00000586153.1:c.330T>A
|
ENSP00000464699.1:p.Pro110=
|
|
ENST00000586336.5:n.783T>A
|
|
|
ENST00000586504.5:c.426-109T>A
|
|
|
ENST00000587377.5:c.*4T>A
|
ENSP00000468343.1:n.*4T>A
|
|
ENST00000587711.5:c.369T>A
|
ENSP00000467459.1:p.Pro123=
|
|
ENST00000587843.5:c.*422T>A
|
ENSP00000465970.1:n.*422T>A
|
|
ENST00000588201.5:c.*675T>A
|
ENSP00000466529.1:n.*675T>A
|
|
ENST00000589543.5:n.641T>A
|
|
|
ENST00000591292.5:n.2013T>A
|
|
|
ENST00000591392.5:c.612T>A
|
ENSP00000467509.1:p.Pro204=
|
|
ENST00000592019.1:c.77-134T>A
|
|
|
NM_024589.2:c.684T>A , LRG_455t1:c.684T>A
|
NP_078865.1:p.Pro228=
|
|
NR_046480.1:n.1008T>A
|
|
|
XM_006720947.2:c.684T>A
|
XP_006721010.1:p.Pro228=
|
|
XM_006720948.2:c.414T>A
|
XP_006721011.1:p.Pro138=
|
|
XM_006720947.4:c.684T>A
|
XP_006721010.1:p.Pro228=
|
|
XM_006720948.4:c.414T>A
|
XP_006721011.1:p.Pro138=
|
|
NM_024589.3:c.684T>A
MANE Select
|
NP_078865.1:p.Pro228=
|
|
NR_046480.2:n.691T>A
|
|
|