ENST00000322048.12:c.662G>C
MANE Select
|
ENSP00000322832.6:p.Gly221Ala
|
|
ENST00000322048.11:c.662G>C
|
ENSP00000322832.5:p.Gly221Ala
|
|
ENST00000586153.1:c.308G>C
|
ENSP00000464699.1:p.Gly103Ala
|
|
ENST00000586336.5:n.761G>C
|
|
|
ENST00000586504.5:c.425+100G>C
|
|
|
ENST00000587377.5:c.675G>C
|
ENSP00000468343.1:p.Trp225Cys
|
|
ENST00000587711.5:c.347G>C
|
ENSP00000467459.1:p.Gly116Ala
|
|
ENST00000587843.5:c.*400G>C
|
ENSP00000465970.1:n.*400G>C
|
|
ENST00000588201.5:c.*653G>C
|
ENSP00000466529.1:n.*653G>C
|
|
ENST00000589543.5:n.619G>C
|
|
|
ENST00000591292.5:n.1991G>C
|
|
|
ENST00000591392.5:c.590G>C
|
ENSP00000467509.1:p.Gly197Ala
|
|
ENST00000592019.1:c.77-156G>C
|
|
|
NM_024589.2:c.662G>C , LRG_455t1:c.662G>C
|
NP_078865.1:p.Gly221Ala
|
|
NR_046480.1:n.986G>C
|
|
|
XM_006720947.2:c.662G>C
|
XP_006721010.1:p.Gly221Ala
|
|
XM_006720948.2:c.392G>C
|
XP_006721011.1:p.Gly131Ala
|
|
XM_006720947.4:c.662G>C
|
XP_006721010.1:p.Gly221Ala
|
|
XM_006720948.4:c.392G>C
|
XP_006721011.1:p.Gly131Ala
|
|
NM_024589.3:c.662G>C
MANE Select
|
NP_078865.1:p.Gly221Ala
|
|
NR_046480.2:n.669G>C
|
|
|