ENST00000205402.10:c.820T>G
MANE Select
|
ENSP00000205402.3:p.Leu274Val
|
|
ENST00000205402.9:c.820T>G
|
ENSP00000205402.3:p.Leu274Val
|
|
ENST00000415325.5:c.*494T>G
|
ENSP00000402593.1:n.*494T>G
|
|
ENST00000417551.5:c.820T>G
|
ENSP00000390667.1:p.Leu274Val
|
|
ENST00000437604.6:c.676T>G
|
ENSP00000387542.2:p.Leu226Val
|
|
ENST00000440410.5:c.751T>G
|
ENSP00000417016.1:p.Leu251Val
|
|
NM_000108.4:c.820T>G
|
NP_000099.2:p.Leu274Val
|
|
NM_001289750.1:c.523T>G
|
NP_001276679.1:p.Leu175Val
|
|
NM_001289751.1:c.751T>G
|
NP_001276680.1:p.Leu251Val
|
|
NM_001289752.1:c.676T>G
|
NP_001276681.1:p.Leu226Val
|
|
NM_000108.5:c.820T>G
MANE Select
|
NP_000099.2:p.Leu274Val
|
|