ENST00000295897.9:c.1118T>A
MANE Select
|
ENSP00000295897.4:p.Leu373His
|
|
ENST00000295897.8:c.1118T>A
|
ENSP00000295897.4:p.Leu373His
|
|
ENST00000401494.7:c.773T>A
|
ENSP00000384695.3:p.Leu258His
|
|
ENST00000415165.6:c.542T>A
|
ENSP00000401820.2:p.Leu181His
|
|
ENST00000476441.6:c.*397T>A
|
ENSP00000423727.1:n.*397T>A
|
|
ENST00000484992.1:n.438T>A
|
|
|
ENST00000503124.5:c.668T>A
|
ENSP00000421027.1:p.Leu223His
|
|
ENST00000504043.1:n.121T>A
|
|
|
ENST00000505649.5:n.804T>A
|
|
|
ENST00000509063.5:c.1118T>A
|
ENSP00000422784.1:p.Leu373His
|
|
ENST00000511370.1:c.651T>A
|
|
|
ENST00000621085.4:c.491-12T>A
|
ENSP00000483421.1:n.491-12T>A
|
|
ENST00000621628.4:c.487-8T>A
|
ENSP00000480485.1:n.487-8T>A
|
|
NM_000477.5:c.1118T>A
|
NP_000468.1:p.Leu373His
|
|
NM_000477.6:c.1118T>A
|
NP_000468.1:p.Leu373His
|
|
NM_000477.7:c.1118T>A
MANE Select
|
NP_000468.1:p.Leu373His
|
|