ENST00000311549.11:c.84C>G
MANE Select
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ENSP00000346027.4:p.Ala28=
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ENST00000272274.8:c.84C>G
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ENSP00000351021.2:p.Ala28=
|
|
ENST00000311549.10:c.84C>G
|
ENSP00000346027.4:p.Ala28=
|
|
ENST00000319826.8:c.84C>G
|
ENSP00000370574.1:p.Ala28=
|
|
ENST00000326092.8:c.84C>G
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ENSP00000370569.1:p.Ala28=
|
|
ENST00000461690.5:c.84C>G
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ENSP00000434298.1:p.Ala28=
|
|
ENST00000466550.1:n.96C>G
|
|
|
ENST00000473558.5:n.320C>G
|
|
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ENST00000483765.5:c.67+393C>G
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ENSP00000473246.1:n.67+393C>G
|
|
ENST00000493317.1:c.84C>G
|
ENSP00000471695.1:p.Ala28=
|
|
NM_000982.3:c.84C>G
|
NP_000973.2:p.Ala28=
|
|
NM_000982.4:c.84C>G
MANE Select
|
NP_000973.2:p.Ala28=
|
|