ENST00000333213.11:c.*273G>C
MANE Select
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ENSP00000327487.6:n.*273G>C
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ENST00000434205.8:c.*273G>C
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ENSP00000406559.4:n.*273G>C
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ENST00000545228.3:c.*353G>C
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ENSP00000438169.3:n.*353G>C
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ENST00000577197.2:n.1052G>C
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ENST00000579449.2:n.2594G>C
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ENST00000580013.6:n.2998G>C
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|
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ENST00000679370.1:n.3376G>C
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ENST00000679429.1:c.*1312G>C
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ENSP00000505403.1:n.*1312G>C
|
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ENST00000679443.1:n.1923G>C
|
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ENST00000679782.1:c.*553G>C
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ENSP00000505995.1:n.*553G>C
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ENST00000679919.1:n.2125G>C
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ENST00000679928.1:c.*2406G>C
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ENSP00000506071.1:n.*2406G>C
|
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ENST00000680999.1:c.*273G>C
|
ENSP00000504984.1:n.*273G>C
|
|
ENST00000681282.1:c.*2041G>C
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ENSP00000506339.1:n.*2041G>C
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ENST00000333213.10:c.*273G>C
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ENSP00000327487.6:n.*273G>C
|
|
ENST00000545228.2:c.1131G>C
|
|
|
ENST00000577197.1:n.602G>C
|
|
|
NM_207346.2:c.*273G>C
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NP_997229.2:n.*273G>C
|
|
XM_005257229.2:c.*353G>C
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XP_005257286.1:n.*353G>C
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XM_006721821.2:c.*353G>C
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XP_006721884.1:n.*353G>C
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XM_011524616.1:c.*353G>C
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XP_011522918.1:n.*353G>C
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XM_011524618.1:c.*273G>C
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XP_011522920.1:n.*273G>C
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XR_243646.2:n.2086G>C
|
|
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XM_005257229.4:c.*353G>C
|
XP_005257286.1:n.*353G>C
|
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XR_243646.4:n.2092G>C
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|
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NM_207346.3:c.*273G>C
MANE Select
|
NP_997229.2:n.*273G>C
|
|