ENST00000262891.9:c.*641A>C
MANE Select
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ENSP00000262891.3:n.*641A>C
|
|
ENST00000262891.8:c.*641A>C
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ENSP00000262891.3:n.*641A>C
|
|
ENST00000300843.8:c.*913A>C
|
ENSP00000300843.3:n.*913A>C
|
|
ENST00000620044.4:c.*1279A>C
|
ENSP00000480702.1:n.*1279A>C
|
|
ENST00000622871.1:c.*641A>C
|
ENSP00000484974.1:n.*641A>C
|
|
NM_001199867.1:c.*641A>C
|
NP_001186796.1:n.*641A>C
|
|
NM_031417.3:c.*913A>C
|
NP_113605.2:n.*913A>C
|
|
XM_006723307.2:c.*641A>C
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XP_006723370.1:n.*641A>C
|
|
XM_006723307.4:c.*641A>C
|
XP_006723370.1:n.*641A>C
|
|
NM_001199867.2:c.*641A>C
MANE Select
|
NP_001186796.1:n.*641A>C
|
|
NM_031417.4:c.*913A>C
|
NP_113605.2:n.*913A>C
|
|