ENST00000264595.7:c.394+311G>T
MANE Select
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ENSP00000264595.2:n.394+311G>T
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ENST00000264595.6:c.394+311G>T
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ENSP00000264595.2:n.394+311G>T
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ENST00000502310.5:c.49+311G>T
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ENSP00000423798.1:n.49+311G>T
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ENST00000506853.5:n.428+311G>T
|
|
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ENST00000510635.1:c.90+311G>T
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ENST00000510955.5:n.316-408G>T
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|
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NM_000027.3:c.394+311G>T
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NP_000018.2:n.394+311G>T
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NM_001171988.1:c.394+311G>T
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NP_001165459.1:n.394+311G>T
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NR_033655.1:n.522+311G>T
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|
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XM_006714123.2:c.394+311G>T
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XP_006714186.1:n.394+311G>T
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XR_001741155.2:n.488+311G>T
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|
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NM_000027.4:c.394+311G>T
MANE Select
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NP_000018.2:n.394+311G>T
|
|
NM_001171988.2:c.394+311G>T
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NP_001165459.1:n.394+311G>T
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NR_033655.2:n.456+311G>T
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