ENST00000295897.9:c.1064T>G
MANE Select
|
ENSP00000295897.4:p.Leu355Trp
|
|
ENST00000295897.8:c.1064T>G
|
ENSP00000295897.4:p.Leu355Trp
|
|
ENST00000401494.7:c.719T>G
|
ENSP00000384695.3:p.Leu240Trp
|
|
ENST00000415165.6:c.488T>G
|
ENSP00000401820.2:p.Leu163Trp
|
|
ENST00000476441.6:c.*343T>G
|
ENSP00000423727.1:n.*343T>G
|
|
ENST00000484992.1:n.384T>G
|
|
|
ENST00000503124.5:c.614T>G
|
ENSP00000421027.1:p.Leu205Trp
|
|
ENST00000504043.1:n.67T>G
|
|
|
ENST00000505649.5:n.750T>G
|
|
|
ENST00000509063.5:c.1064T>G
|
ENSP00000422784.1:p.Leu355Trp
|
|
ENST00000511370.1:c.597T>G
|
|
|
ENST00000621085.4:c.491-66T>G
|
ENSP00000483421.1:n.491-66T>G
|
|
ENST00000621628.4:c.487-62T>G
|
ENSP00000480485.1:n.487-62T>G
|
|
NM_000477.5:c.1064T>G
|
NP_000468.1:p.Leu355Trp
|
|
NM_000477.6:c.1064T>G
|
NP_000468.1:p.Leu355Trp
|
|
NM_000477.7:c.1064T>G
MANE Select
|
NP_000468.1:p.Leu355Trp
|
|