ENST00000295897.9:c.1819T>G
MANE Select
|
ENSP00000295897.4:p.Leu607Val
|
|
ENST00000295897.8:c.1819T>G
|
ENSP00000295897.4:p.Leu607Val
|
|
ENST00000401494.7:c.1474T>G
|
ENSP00000384695.3:p.Leu492Val
|
|
ENST00000415165.6:c.1243T>G
|
ENSP00000401820.2:p.Leu415Val
|
|
ENST00000476441.6:c.*1098T>G
|
ENSP00000423727.1:n.*1098T>G
|
|
ENST00000495173.1:n.127T>G
|
|
|
ENST00000503124.5:c.1369T>G
|
ENSP00000421027.1:p.Leu457Val
|
|
ENST00000505649.5:n.1366T>G
|
|
|
ENST00000508932.5:n.209T>G
|
|
|
ENST00000509063.5:c.1785+648T>G
|
ENSP00000422784.1:n.1785+648T>G
|
|
ENST00000511370.1:c.1352T>G
|
|
|
ENST00000621085.4:c.1180T>G
|
ENSP00000483421.1:p.Leu394Val
|
|
ENST00000621628.4:c.1180T>G
|
ENSP00000480485.1:p.Leu394Val
|
|
NM_000477.5:c.1819T>G
|
NP_000468.1:p.Leu607Val
|
|
NM_000477.6:c.1819T>G
|
NP_000468.1:p.Leu607Val
|
|
NM_000477.7:c.1819T>G
MANE Select
|
NP_000468.1:p.Leu607Val
|
|