ENST00000333213.11:c.*253T>A
MANE Select
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ENSP00000327487.6:n.*253T>A
|
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ENST00000434205.8:c.*253T>A
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ENSP00000406559.4:n.*253T>A
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ENST00000545228.3:c.*333T>A
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ENSP00000438169.3:n.*333T>A
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ENST00000577197.2:n.1032T>A
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ENST00000579449.2:n.2574T>A
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ENST00000580013.6:n.2978T>A
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ENST00000679370.1:n.3356T>A
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ENST00000679429.1:c.*1292T>A
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ENSP00000505403.1:n.*1292T>A
|
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ENST00000679443.1:n.1903T>A
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ENST00000679782.1:c.*533T>A
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ENSP00000505995.1:n.*533T>A
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ENST00000679919.1:n.2105T>A
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ENST00000679928.1:c.*2386T>A
|
ENSP00000506071.1:n.*2386T>A
|
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ENST00000680999.1:c.*253T>A
|
ENSP00000504984.1:n.*253T>A
|
|
ENST00000681282.1:c.*2021T>A
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ENSP00000506339.1:n.*2021T>A
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ENST00000333213.10:c.*253T>A
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ENSP00000327487.6:n.*253T>A
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ENST00000545228.2:c.1111T>A
|
|
|
ENST00000577197.1:n.582T>A
|
|
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NM_207346.2:c.*253T>A
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NP_997229.2:n.*253T>A
|
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XM_005257229.2:c.*333T>A
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XP_005257286.1:n.*333T>A
|
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XM_006721821.2:c.*333T>A
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XP_006721884.1:n.*333T>A
|
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XM_011524616.1:c.*333T>A
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XP_011522918.1:n.*333T>A
|
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XM_011524618.1:c.*253T>A
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XP_011522920.1:n.*253T>A
|
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XR_243646.2:n.2066T>A
|
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XM_005257229.4:c.*333T>A
|
XP_005257286.1:n.*333T>A
|
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XR_243646.4:n.2072T>A
|
|
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NM_207346.3:c.*253T>A
MANE Select
|
NP_997229.2:n.*253T>A
|
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