ENST00000261647.10:c.1005A>G
MANE Select
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ENSP00000261647.5:p.Thr335=
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ENST00000261647.9:c.1005A>G
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ENSP00000261647.5:p.Thr335=
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ENST00000465567.1:n.1399A>G
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|
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ENST00000470649.1:c.247+682A>G
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ENSP00000465627.1:n.247+682A>G
|
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ENST00000475723.5:c.1189A>G
|
|
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ENST00000481107.1:n.1673A>G
|
|
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ENST00000497842.6:n.1209A>G
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|
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NM_001271420.1:c.684A>G
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NP_001258349.1:p.Thr228=
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NM_017775.3:c.1005A>G
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NP_060245.3:p.Thr335=
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XM_017024801.2:c.994+682A>G
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XP_016880290.2:n.994+682A>G
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XM_017024802.2:c.994+682A>G
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XP_016880291.2:n.994+682A>G
|
|
NM_017775.4:c.1005A>G
MANE Select
|
NP_060245.3:p.Thr335=
|
|
NM_001271420.2:c.684A>G
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NP_001258349.1:p.Thr228=
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