ENST00000322344.8:c.1313C>G
MANE Select
|
ENSP00000323511.2:p.Ala438Gly
|
|
ENST00000322344.7:c.1313C>G
|
ENSP00000323511.2:p.Ala438Gly
|
|
ENST00000593946.5:c.*1240C>G
|
ENSP00000468896.1:n.*1240C>G
|
|
ENST00000594661.5:n.1814C>G
|
|
|
ENST00000595081.5:n.216C>G
|
|
|
ENST00000596014.5:c.1313C>G
|
ENSP00000472300.1:p.Ala438Gly
|
|
ENST00000597965.2:c.20C>G
|
ENSP00000471097.2:p.Ala7Gly
|
|
ENST00000599454.5:n.233C>G
|
|
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ENST00000600573.5:c.1220C>G
|
ENSP00000469826.1:p.Ala407Gly
|
|
ENST00000600910.5:c.1203C>G
|
ENSP00000473137.1:p.Cys401Trp
|
|
ENST00000601816.3:n.288C>G
|
|
|
ENST00000625216.2:c.394C>G
|
ENSP00000486898.1:n.394C>G
|
|
ENST00000627232.2:c.1233C>G
|
ENSP00000486037.1:n.1233C>G
|
|
ENST00000631020.2:c.1205C>G
|
ENSP00000486707.1:p.Ala402Gly
|
|
NM_007254.3:c.1313C>G
|
NP_009185.2:p.Ala438Gly
|
|
NM_007254.4:c.1313C>G
MANE Select
|
NP_009185.2:p.Ala438Gly
|
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