ENST00000695651.1:n.2159G>T
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ENST00000695653.1:c.1720G>T
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ENSP00000512084.1:p.Ala574Ser
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ENST00000695654.1:c.2836G>T
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ENSP00000512085.1:p.Ala946Ser
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ENST00000695690.1:n.2G>T
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ENST00000695691.1:n.2G>T
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ENST00000245907.11:c.3811G>T
MANE Select
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ENSP00000245907.4:p.Ala1271Ser
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ENST00000245907.10:c.3811G>T
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ENSP00000245907.4:p.Ala1271Ser
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ENST00000596238.1:n.254G>T
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ENST00000601008.1:c.241+1600G>T
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ENSP00000471384.1:n.241+1600G>T
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NM_000064.3:c.3811G>T
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NP_000055.2:p.Ala1271Ser
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NM_000064.4:c.3811G>T
MANE Select
|
NP_000055.2:p.Ala1271Ser
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