ENST00000333213.11:c.1456T>C
MANE Select
|
ENSP00000327487.6:p.Cys486Arg
|
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ENST00000434205.8:c.1153T>C
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ENSP00000406559.4:p.Cys385Arg
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ENST00000545228.3:c.1644T>C
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ENSP00000438169.3:p.Ser548=
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ENST00000577197.2:n.654T>C
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|
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ENST00000579449.2:n.2196T>C
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|
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ENST00000580013.6:n.2600T>C
|
|
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ENST00000679370.1:n.2978T>C
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|
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ENST00000679429.1:c.*914T>C
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ENSP00000505403.1:n.*914T>C
|
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ENST00000679443.1:n.1525T>C
|
|
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ENST00000679782.1:c.*155T>C
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ENSP00000505995.1:n.*155T>C
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ENST00000679919.1:n.1727T>C
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|
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ENST00000679928.1:c.*2008T>C
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ENSP00000506071.1:n.*2008T>C
|
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ENST00000680528.1:n.2422T>C
|
|
|
ENST00000680999.1:c.1669T>C
|
ENSP00000504984.1:p.Cys557Arg
|
|
ENST00000681282.1:c.*1643T>C
|
ENSP00000506339.1:n.*1643T>C
|
|
ENST00000333213.10:c.1456T>C
|
ENSP00000327487.6:p.Cys486Arg
|
|
ENST00000545228.2:c.733T>C
|
|
|
ENST00000577197.1:n.204T>C
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|
|
ENST00000579449.1:n.653T>C
|
|
|
NM_207346.2:c.1456T>C
|
NP_997229.2:p.Cys486Arg
|
|
XM_005257229.2:c.1644T>C
|
XP_005257286.1:p.Ser548=
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XM_006721821.2:c.1341T>C
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XP_006721884.1:p.Ser447=
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XM_011524616.1:c.1527T>C
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XP_011522918.1:p.Ser509=
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XM_011524617.1:c.*38T>C
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XP_011522919.1:n.*38T>C
|
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XM_011524618.1:c.1339T>C
|
XP_011522920.1:p.Cys447Arg
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|
XR_243646.2:n.1688T>C
|
|
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XM_005257229.4:c.1644T>C
|
XP_005257286.1:p.Ser548=
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XR_001753015.1:n.87+24A>G
|
|
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XR_001753016.1:n.88+24A>G
|
|
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XR_243646.4:n.1694T>C
|
|
|
NM_207346.3:c.1456T>C
MANE Select
|
NP_997229.2:p.Cys486Arg
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