ENST00000295897.9:c.1455T=
MANE Select
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ENSP00000295897.4:p.Cys485=
|
|
ENST00000295897.8:c.1455T=
|
ENSP00000295897.4:p.Cys485=
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|
ENST00000401494.7:c.1110T=
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ENSP00000384695.3:p.Cys370=
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|
ENST00000415165.6:c.879T=
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ENSP00000401820.2:p.Cys293=
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|
ENST00000476441.6:c.*734T=
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ENSP00000423727.1:n.*734T=
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|
ENST00000486939.1:n.109T=
|
|
|
ENST00000503124.5:c.1005T=
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ENSP00000421027.1:p.Cys335=
|
|
ENST00000505649.5:n.1002T=
|
|
|
ENST00000509063.5:c.1455T=
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ENSP00000422784.1:p.Cys485=
|
|
ENST00000511370.1:c.988T=
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|
|
ENST00000621085.4:c.816T=
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ENSP00000483421.1:p.Cys272=
|
|
ENST00000621628.4:c.816T=
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ENSP00000480485.1:p.Cys272=
|
|
NM_000477.5:c.1455T=
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NP_000468.1:p.Cys485=
|
|
NM_000477.6:c.1455T=
|
NP_000468.1:p.Cys485=
|
|
NM_000477.7:c.1455T=
MANE Select
|
NP_000468.1:p.Cys485=
|
|