ENST00000322048.12:c.363C>T
MANE Select
|
ENSP00000322832.6:p.Ser121=
|
|
ENST00000322048.11:c.363C>T
|
ENSP00000322832.5:p.Ser121=
|
|
ENST00000585653.1:n.495C>T
|
|
|
ENST00000586153.1:c.108C>T
|
ENSP00000464699.1:p.Ser36=
|
|
ENST00000586336.5:n.462C>T
|
|
|
ENST00000586504.5:c.143C>T
|
|
|
ENST00000587377.5:c.363C>T
|
ENSP00000468343.1:p.Ser121=
|
|
ENST00000587711.5:c.118-1088C>T
|
ENSP00000467459.1:n.118-1088C>T
|
|
ENST00000587843.5:c.*101C>T
|
ENSP00000465970.1:n.*101C>T
|
|
ENST00000588201.5:c.*220C>T
|
ENSP00000466529.1:n.*220C>T
|
|
ENST00000589543.5:n.320C>T
|
|
|
ENST00000591292.5:n.1692C>T
|
|
|
ENST00000591392.5:c.291C>T
|
ENSP00000467509.1:p.Ser97=
|
|
ENST00000592019.1:c.76+6C>T
|
|
|
NM_024589.2:c.363C>T , LRG_455t1:c.363C>T
|
NP_078865.1:p.Ser121=
|
|
NR_046480.1:n.687C>T
|
|
|
XM_006720947.2:c.363C>T
|
XP_006721010.1:p.Ser121=
|
|
XM_006720948.2:c.93C>T
|
XP_006721011.1:p.Ser31=
|
|
XM_006720947.4:c.363C>T
|
XP_006721010.1:p.Ser121=
|
|
XM_006720948.4:c.93C>T
|
XP_006721011.1:p.Ser31=
|
|
NM_024589.3:c.363C>T
MANE Select
|
NP_078865.1:p.Ser121=
|
|
NR_046480.2:n.370C>T
|
|
|