ENST00000322048.12:c.611A>C
MANE Select
|
ENSP00000322832.6:p.Tyr204Ser
|
|
ENST00000322048.11:c.611A>C
|
ENSP00000322832.5:p.Tyr204Ser
|
|
ENST00000586153.1:c.257A>C
|
ENSP00000464699.1:p.Tyr86Ser
|
|
ENST00000586336.5:n.710A>C
|
|
|
ENST00000586504.5:c.391A>C
|
|
|
ENST00000587377.5:c.624A>C
|
ENSP00000468343.1:p.Val208=
|
|
ENST00000587711.5:c.296A>C
|
ENSP00000467459.1:p.Tyr99Ser
|
|
ENST00000587843.5:c.*349A>C
|
ENSP00000465970.1:n.*349A>C
|
|
ENST00000588201.5:c.*602A>C
|
ENSP00000466529.1:n.*602A>C
|
|
ENST00000589543.5:n.568A>C
|
|
|
ENST00000591292.5:n.1940A>C
|
|
|
ENST00000591392.5:c.539A>C
|
ENSP00000467509.1:p.Tyr180Ser
|
|
ENST00000592019.1:c.77-290A>C
|
|
|
NM_024589.2:c.611A>C , LRG_455t1:c.611A>C
|
NP_078865.1:p.Tyr204Ser
|
|
NR_046480.1:n.935A>C
|
|
|
XM_006720947.2:c.611A>C
|
XP_006721010.1:p.Tyr204Ser
|
|
XM_006720948.2:c.341A>C
|
XP_006721011.1:p.Tyr114Ser
|
|
XM_006720947.4:c.611A>C
|
XP_006721010.1:p.Tyr204Ser
|
|
XM_006720948.4:c.341A>C
|
XP_006721011.1:p.Tyr114Ser
|
|
NM_024589.3:c.611A>C
MANE Select
|
NP_078865.1:p.Tyr204Ser
|
|
NR_046480.2:n.618A>C
|
|
|