ENST00000322048.12:c.418G=
MANE Select
|
ENSP00000322832.6:p.Ala140=
|
|
ENST00000322048.11:c.418G=
|
ENSP00000322832.5:p.Ala140=
|
|
ENST00000585653.1:n.550G=
|
|
|
ENST00000586153.1:c.163G=
|
ENSP00000464699.1:p.Ala55=
|
|
ENST00000586336.5:n.517G=
|
|
|
ENST00000586504.5:c.198G=
|
|
|
ENST00000587377.5:c.418G=
|
ENSP00000468343.1:p.Ala140=
|
|
ENST00000587711.5:c.118-1033G=
|
ENSP00000467459.1:n.118-1033G=
|
|
ENST00000587843.5:c.*156G=
|
ENSP00000465970.1:n.*156G=
|
|
ENST00000588201.5:c.*275G=
|
ENSP00000466529.1:n.*275G=
|
|
ENST00000589543.5:n.375G=
|
|
|
ENST00000591292.5:n.1747G=
|
|
|
ENST00000591392.5:c.346G=
|
ENSP00000467509.1:p.Ala116=
|
|
ENST00000592019.1:c.76+61G=
|
|
|
NM_024589.2:c.418G= , LRG_455t1:c.418G=
|
NP_078865.1:p.Ala140=
|
|
NR_046480.1:n.742G=
|
|
|
XM_006720947.2:c.418G=
|
XP_006721010.1:p.Ala140=
|
|
XM_006720948.2:c.148G=
|
XP_006721011.1:p.Ala50=
|
|
XM_006720947.4:c.418G=
|
XP_006721010.1:p.Ala140=
|
|
XM_006720948.4:c.148G=
|
XP_006721011.1:p.Ala50=
|
|
NM_024589.3:c.418G=
MANE Select
|
NP_078865.1:p.Ala140=
|
|
NR_046480.2:n.425G=
|
|
|