ENST00000295897.9:c.1825T>G
MANE Select
|
ENSP00000295897.4:p.Leu609Val
|
|
ENST00000295897.8:c.1825T>G
|
ENSP00000295897.4:p.Leu609Val
|
|
ENST00000401494.7:c.1480T>G
|
ENSP00000384695.3:p.Leu494Val
|
|
ENST00000415165.6:c.1249T>G
|
ENSP00000401820.2:p.Leu417Val
|
|
ENST00000476441.6:c.*1104T>G
|
ENSP00000423727.1:n.*1104T>G
|
|
ENST00000495173.1:n.133T>G
|
|
|
ENST00000503124.5:c.1375T>G
|
ENSP00000421027.1:p.Leu459Val
|
|
ENST00000505649.5:n.1372T>G
|
|
|
ENST00000508932.5:n.215T>G
|
|
|
ENST00000509063.5:c.1785+654T>G
|
ENSP00000422784.1:n.1785+654T>G
|
|
ENST00000511370.1:c.1358T>G
|
|
|
ENST00000621085.4:c.1186T>G
|
ENSP00000483421.1:p.Leu396Val
|
|
ENST00000621628.4:c.1186T>G
|
ENSP00000480485.1:p.Leu396Val
|
|
NM_000477.5:c.1825T>G
|
NP_000468.1:p.Leu609Val
|
|
NM_000477.6:c.1825T>G
|
NP_000468.1:p.Leu609Val
|
|
NM_000477.7:c.1825T>G
MANE Select
|
NP_000468.1:p.Leu609Val
|
|