ENST00000609686.4:c.412-177C=
MANE Select
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ENSP00000477455.1:n.412-177C=
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ENST00000630791.2:c.412-177C=
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ENSP00000486677.2:n.412-177C=
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ENST00000609686.3:c.412-177C=
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ENSP00000477455.1:n.412-177C=
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NM_000834.3:c.412-177C=
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NP_000825.2:n.412-177C=
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XM_011520628.1:c.412-177C=
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XP_011518930.1:n.412-177C=
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XM_011520629.1:c.412-177C=
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XP_011518931.1:n.412-177C=
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XM_011520630.1:c.412-177C=
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XP_011518932.1:n.412-177C=
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NM_000834.4:c.412-177C=
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NP_000825.2:n.412-177C=
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XM_011520628.2:c.412-177C=
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XP_011518930.1:n.412-177C=
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XM_011520629.2:c.412-177C=
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XP_011518931.1:n.412-177C=
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XM_017019219.2:c.412-177C=
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XP_016874708.1:n.412-177C=
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NM_000834.5:c.412-177C=
MANE Select
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NP_000825.2:n.412-177C=
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