ENST00000295897.9:c.1117C>G
MANE Select
|
ENSP00000295897.4:p.Leu373Val
|
|
ENST00000295897.8:c.1117C>G
|
ENSP00000295897.4:p.Leu373Val
|
|
ENST00000401494.7:c.772C>G
|
ENSP00000384695.3:p.Leu258Val
|
|
ENST00000415165.6:c.541C>G
|
ENSP00000401820.2:p.Leu181Val
|
|
ENST00000476441.6:c.*396C>G
|
ENSP00000423727.1:n.*396C>G
|
|
ENST00000484992.1:n.437C>G
|
|
|
ENST00000503124.5:c.667C>G
|
ENSP00000421027.1:p.Leu223Val
|
|
ENST00000504043.1:n.120C>G
|
|
|
ENST00000505649.5:n.803C>G
|
|
|
ENST00000509063.5:c.1117C>G
|
ENSP00000422784.1:p.Leu373Val
|
|
ENST00000511370.1:c.650C>G
|
|
|
ENST00000621085.4:c.491-13C>G
|
ENSP00000483421.1:n.491-13C>G
|
|
ENST00000621628.4:c.487-9C>G
|
ENSP00000480485.1:n.487-9C>G
|
|
NM_000477.5:c.1117C>G
|
NP_000468.1:p.Leu373Val
|
|
NM_000477.6:c.1117C>G
|
NP_000468.1:p.Leu373Val
|
|
NM_000477.7:c.1117C>G
MANE Select
|
NP_000468.1:p.Leu373Val
|
|