ENST00000295897.9:c.1091A>T
MANE Select
|
ENSP00000295897.4:p.Asp364Val
|
|
ENST00000295897.8:c.1091A>T
|
ENSP00000295897.4:p.Asp364Val
|
|
ENST00000401494.7:c.746A>T
|
ENSP00000384695.3:p.Asp249Val
|
|
ENST00000415165.6:c.515A>T
|
ENSP00000401820.2:p.Asp172Val
|
|
ENST00000476441.6:c.*370A>T
|
ENSP00000423727.1:n.*370A>T
|
|
ENST00000484992.1:n.411A>T
|
|
|
ENST00000503124.5:c.641A>T
|
ENSP00000421027.1:p.Asp214Val
|
|
ENST00000504043.1:n.94A>T
|
|
|
ENST00000505649.5:n.777A>T
|
|
|
ENST00000509063.5:c.1091A>T
|
ENSP00000422784.1:p.Asp364Val
|
|
ENST00000511370.1:c.624A>T
|
|
|
ENST00000621085.4:c.491-39A>T
|
ENSP00000483421.1:n.491-39A>T
|
|
ENST00000621628.4:c.487-35A>T
|
ENSP00000480485.1:n.487-35A>T
|
|
NM_000477.5:c.1091A>T
|
NP_000468.1:p.Asp364Val
|
|
NM_000477.6:c.1091A>T
|
NP_000468.1:p.Asp364Val
|
|
NM_000477.7:c.1091A>T
MANE Select
|
NP_000468.1:p.Asp364Val
|
|