ENST00000295897.9:c.1499G>A
MANE Select
|
ENSP00000295897.4:p.Cys500Tyr
|
|
ENST00000295897.8:c.1499G>A
|
ENSP00000295897.4:p.Cys500Tyr
|
|
ENST00000401494.7:c.1154G>A
|
ENSP00000384695.3:p.Cys385Tyr
|
|
ENST00000415165.6:c.923G>A
|
ENSP00000401820.2:p.Cys308Tyr
|
|
ENST00000476441.6:c.*778G>A
|
ENSP00000423727.1:n.*778G>A
|
|
ENST00000486939.1:n.153G>A
|
|
|
ENST00000503124.5:c.1049G>A
|
ENSP00000421027.1:p.Cys350Tyr
|
|
ENST00000505649.5:n.1046G>A
|
|
|
ENST00000509063.5:c.1499G>A
|
ENSP00000422784.1:p.Cys500Tyr
|
|
ENST00000511370.1:c.1032G>A
|
|
|
ENST00000621085.4:c.860G>A
|
ENSP00000483421.1:p.Cys287Tyr
|
|
ENST00000621628.4:c.860G>A
|
ENSP00000480485.1:p.Cys287Tyr
|
|
NM_000477.5:c.1499G>A
|
NP_000468.1:p.Cys500Tyr
|
|
NM_000477.6:c.1499G>A
|
NP_000468.1:p.Cys500Tyr
|
|
NM_000477.7:c.1499G>A
MANE Select
|
NP_000468.1:p.Cys500Tyr
|
|