ENST00000295897.9:c.1817C>G
MANE Select
|
ENSP00000295897.4:p.Ala606Gly
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ENST00000295897.8:c.1817C>G
|
ENSP00000295897.4:p.Ala606Gly
|
|
ENST00000401494.7:c.1472C>G
|
ENSP00000384695.3:p.Ala491Gly
|
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ENST00000415165.6:c.1241C>G
|
ENSP00000401820.2:p.Ala414Gly
|
|
ENST00000476441.6:c.*1096C>G
|
ENSP00000423727.1:n.*1096C>G
|
|
ENST00000495173.1:n.125C>G
|
|
|
ENST00000503124.5:c.1367C>G
|
ENSP00000421027.1:p.Ala456Gly
|
|
ENST00000505649.5:n.1364C>G
|
|
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ENST00000508932.5:n.207C>G
|
|
|
ENST00000509063.5:c.1785+646C>G
|
ENSP00000422784.1:n.1785+646C>G
|
|
ENST00000511370.1:c.1350C>G
|
|
|
ENST00000621085.4:c.1178C>G
|
ENSP00000483421.1:p.Ala393Gly
|
|
ENST00000621628.4:c.1178C>G
|
ENSP00000480485.1:p.Ala393Gly
|
|
NM_000477.5:c.1817C>G
|
NP_000468.1:p.Ala606Gly
|
|
NM_000477.6:c.1817C>G
|
NP_000468.1:p.Ala606Gly
|
|
NM_000477.7:c.1817C>G
MANE Select
|
NP_000468.1:p.Ala606Gly
|
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