ENST00000295897.9:c.1076C>G
MANE Select
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ENSP00000295897.4:p.Ala359Gly
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ENST00000295897.8:c.1076C>G
|
ENSP00000295897.4:p.Ala359Gly
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ENST00000401494.7:c.731C>G
|
ENSP00000384695.3:p.Ala244Gly
|
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ENST00000415165.6:c.500C>G
|
ENSP00000401820.2:p.Ala167Gly
|
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ENST00000476441.6:c.*355C>G
|
ENSP00000423727.1:n.*355C>G
|
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ENST00000484992.1:n.396C>G
|
|
|
ENST00000503124.5:c.626C>G
|
ENSP00000421027.1:p.Ala209Gly
|
|
ENST00000504043.1:n.79C>G
|
|
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ENST00000505649.5:n.762C>G
|
|
|
ENST00000509063.5:c.1076C>G
|
ENSP00000422784.1:p.Ala359Gly
|
|
ENST00000511370.1:c.609C>G
|
|
|
ENST00000621085.4:c.491-54C>G
|
ENSP00000483421.1:n.491-54C>G
|
|
ENST00000621628.4:c.487-50C>G
|
ENSP00000480485.1:n.487-50C>G
|
|
NM_000477.5:c.1076C>G
|
NP_000468.1:p.Ala359Gly
|
|
NM_000477.6:c.1076C>G
|
NP_000468.1:p.Ala359Gly
|
|
NM_000477.7:c.1076C>G
MANE Select
|
NP_000468.1:p.Ala359Gly
|
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