ENST00000264670.11:c.778C>G
MANE Select
|
ENSP00000264670.6:p.Leu260Val
|
|
ENST00000264670.10:c.778C>G
|
ENSP00000264670.6:p.Leu260Val
|
|
ENST00000504374.5:c.*84C>G
|
ENSP00000421783.1:n.*84C>G
|
|
ENST00000505264.1:n.445C>G
|
|
|
ENST00000505892.5:n.1347C>G
|
|
|
ENST00000506139.5:c.673C>G
|
ENSP00000420957.1:p.Leu225Val
|
|
NM_001193455.1:c.673C>G
|
NP_001180384.1:p.Leu225Val
|
|
NM_017755.5:c.778C>G
|
NP_060225.4:p.Leu260Val
|
|
NR_037947.1:n.1074C>G
|
|
|
NM_017755.6:c.778C>G
MANE Select
|
NP_060225.4:p.Leu260Val
|
|
NM_001193455.2:c.673C>G
|
NP_001180384.1:p.Leu225Val
|
|
NR_037947.2:n.758C>G
|
|
|