ENST00000295897.9:c.1139C=
MANE Select
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ENSP00000295897.4:p.Thr380=
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ENST00000295897.8:c.1139C=
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ENSP00000295897.4:p.Thr380=
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|
ENST00000401494.7:c.794C=
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ENSP00000384695.3:p.Thr265=
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|
ENST00000415165.6:c.563C=
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ENSP00000401820.2:p.Thr188=
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ENST00000476441.6:c.*418C=
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ENSP00000423727.1:n.*418C=
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|
ENST00000484992.1:n.459C=
|
|
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ENST00000503124.5:c.689C=
|
ENSP00000421027.1:p.Thr230=
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|
ENST00000504043.1:n.142C=
|
|
|
ENST00000505649.5:n.825C=
|
|
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ENST00000509063.5:c.1139C=
|
ENSP00000422784.1:p.Thr380=
|
|
ENST00000511370.1:c.672C=
|
|
|
ENST00000621085.4:c.500C=
|
ENSP00000483421.1:p.Thr167=
|
|
ENST00000621628.4:c.500C=
|
ENSP00000480485.1:p.Thr167=
|
|
NM_000477.5:c.1139C=
|
NP_000468.1:p.Thr380=
|
|
NM_000477.6:c.1139C=
|
NP_000468.1:p.Thr380=
|
|
NM_000477.7:c.1139C=
MANE Select
|
NP_000468.1:p.Thr380=
|
|