ENST00000295897.9:c.1727C>G
MANE Select
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ENSP00000295897.4:p.Ala576Gly
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ENST00000295897.8:c.1727C>G
|
ENSP00000295897.4:p.Ala576Gly
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ENST00000401494.7:c.1382C>G
|
ENSP00000384695.3:p.Ala461Gly
|
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ENST00000415165.6:c.1151C>G
|
ENSP00000401820.2:p.Ala384Gly
|
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ENST00000476441.6:c.*1006C>G
|
ENSP00000423727.1:n.*1006C>G
|
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ENST00000495173.1:n.35C>G
|
|
|
ENST00000503124.5:c.1277C>G
|
ENSP00000421027.1:p.Ala426Gly
|
|
ENST00000505649.5:n.1274C>G
|
|
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ENST00000508932.5:n.175+126C>G
|
|
|
ENST00000509063.5:c.1727C>G
|
ENSP00000422784.1:p.Ala576Gly
|
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ENST00000511370.1:c.1260C>G
|
|
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ENST00000621085.4:c.1088C>G
|
ENSP00000483421.1:p.Ala363Gly
|
|
ENST00000621628.4:c.1088C>G
|
ENSP00000480485.1:p.Ala363Gly
|
|
NM_000477.5:c.1727C>G
|
NP_000468.1:p.Ala576Gly
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|
NM_000477.6:c.1727C>G
|
NP_000468.1:p.Ala576Gly
|
|
NM_000477.7:c.1727C>G
MANE Select
|
NP_000468.1:p.Ala576Gly
|
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