ENST00000322048.12:c.616C>G
MANE Select
|
ENSP00000322832.6:p.Leu206Val
|
|
ENST00000322048.11:c.616C>G
|
ENSP00000322832.5:p.Leu206Val
|
|
ENST00000586153.1:c.262C>G
|
ENSP00000464699.1:p.Leu88Val
|
|
ENST00000586336.5:n.715C>G
|
|
|
ENST00000586504.5:c.396C>G
|
|
|
ENST00000587377.5:c.629C>G
|
ENSP00000468343.1:p.Ala210Gly
|
|
ENST00000587711.5:c.301C>G
|
ENSP00000467459.1:p.Leu101Val
|
|
ENST00000587843.5:c.*354C>G
|
ENSP00000465970.1:n.*354C>G
|
|
ENST00000588201.5:c.*607C>G
|
ENSP00000466529.1:n.*607C>G
|
|
ENST00000589543.5:n.573C>G
|
|
|
ENST00000591292.5:n.1945C>G
|
|
|
ENST00000591392.5:c.544C>G
|
ENSP00000467509.1:p.Leu182Val
|
|
ENST00000592019.1:c.77-285C>G
|
|
|
NM_024589.2:c.616C>G , LRG_455t1:c.616C>G
|
NP_078865.1:p.Leu206Val
|
|
NR_046480.1:n.940C>G
|
|
|
XM_006720947.2:c.616C>G
|
XP_006721010.1:p.Leu206Val
|
|
XM_006720948.2:c.346C>G
|
XP_006721011.1:p.Leu116Val
|
|
XM_006720947.4:c.616C>G
|
XP_006721010.1:p.Leu206Val
|
|
XM_006720948.4:c.346C>G
|
XP_006721011.1:p.Leu116Val
|
|
NM_024589.3:c.616C>G
MANE Select
|
NP_078865.1:p.Leu206Val
|
|
NR_046480.2:n.623C>G
|
|
|