ENST00000295897.9:c.1656A>T
MANE Select
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ENSP00000295897.4:p.Ala552=
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ENST00000295897.8:c.1656A>T
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ENSP00000295897.4:p.Ala552=
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ENST00000401494.7:c.1311A>T
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ENSP00000384695.3:p.Ala437=
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ENST00000415165.6:c.1080A>T
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ENSP00000401820.2:p.Ala360=
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ENST00000476441.6:c.*935A>T
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ENSP00000423727.1:n.*935A>T
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ENST00000486939.1:n.310A>T
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|
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ENST00000503124.5:c.1206A>T
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ENSP00000421027.1:p.Ala402=
|
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ENST00000505649.5:n.1203A>T
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|
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ENST00000508932.5:n.175+55A>T
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|
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ENST00000509063.5:c.1656A>T
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ENSP00000422784.1:p.Ala552=
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ENST00000511370.1:c.1189A>T
|
|
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ENST00000621085.4:c.1017A>T
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ENSP00000483421.1:p.Ala339=
|
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ENST00000621628.4:c.1017A>T
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ENSP00000480485.1:p.Ala339=
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NM_000477.5:c.1656A>T
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NP_000468.1:p.Ala552=
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NM_000477.6:c.1656A>T
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NP_000468.1:p.Ala552=
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|
NM_000477.7:c.1656A>T
MANE Select
|
NP_000468.1:p.Ala552=
|
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