ENST00000295897.9:c.1620T>G
MANE Select
|
ENSP00000295897.4:p.Leu540=
|
|
ENST00000295897.8:c.1620T>G
|
ENSP00000295897.4:p.Leu540=
|
|
ENST00000401494.7:c.1275T>G
|
ENSP00000384695.3:p.Leu425=
|
|
ENST00000415165.6:c.1044T>G
|
ENSP00000401820.2:p.Leu348=
|
|
ENST00000476441.6:c.*899T>G
|
ENSP00000423727.1:n.*899T>G
|
|
ENST00000486939.1:n.274T>G
|
|
|
ENST00000503124.5:c.1170T>G
|
ENSP00000421027.1:p.Leu390=
|
|
ENST00000505649.5:n.1167T>G
|
|
|
ENST00000509063.5:c.1620T>G
|
ENSP00000422784.1:p.Leu540=
|
|
ENST00000511370.1:c.1153T>G
|
|
|
ENST00000621085.4:c.981T>G
|
ENSP00000483421.1:p.Leu327=
|
|
ENST00000621628.4:c.981T>G
|
ENSP00000480485.1:p.Leu327=
|
|
NM_000477.5:c.1620T>G
|
NP_000468.1:p.Leu540=
|
|
NM_000477.6:c.1620T>G
|
NP_000468.1:p.Leu540=
|
|
NM_000477.7:c.1620T>G
MANE Select
|
NP_000468.1:p.Leu540=
|
|