ENST00000295897.9:c.1128A=
MANE Select
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ENSP00000295897.4:p.Thr376=
|
|
ENST00000295897.8:c.1128A=
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ENSP00000295897.4:p.Thr376=
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|
ENST00000401494.7:c.783A=
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ENSP00000384695.3:p.Thr261=
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|
ENST00000415165.6:c.552A=
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ENSP00000401820.2:p.Thr184=
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ENST00000476441.6:c.*407A=
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ENSP00000423727.1:n.*407A=
|
|
ENST00000484992.1:n.448A=
|
|
|
ENST00000503124.5:c.678A=
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ENSP00000421027.1:p.Thr226=
|
|
ENST00000504043.1:n.131A=
|
|
|
ENST00000505649.5:n.814A=
|
|
|
ENST00000509063.5:c.1128A=
|
ENSP00000422784.1:p.Thr376=
|
|
ENST00000511370.1:c.661A=
|
|
|
ENST00000621085.4:c.491-2A=
|
ENSP00000483421.1:n.491-2A=
|
|
ENST00000621628.4:c.489A=
|
ENSP00000480485.1:p.Thr163=
|
|
NM_000477.5:c.1128A=
|
NP_000468.1:p.Thr376=
|
|
NM_000477.6:c.1128A=
|
NP_000468.1:p.Thr376=
|
|
NM_000477.7:c.1128A=
MANE Select
|
NP_000468.1:p.Thr376=
|
|