ENST00000588860.6:c.1295G=
|
ENSP00000465878.2:p.Ser432=
|
|
ENST00000589076.6:c.1295G=
|
ENSP00000466934.2:p.Ser432=
|
|
ENST00000589941.2:c.1295G=
|
ENSP00000465874.2:p.Ser432=
|
|
ENST00000590061.2:c.1295G=
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ENSP00000464772.2:p.Ser432=
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|
ENST00000593223.2:c.1295G=
|
ENSP00000466118.2:p.Ser432=
|
|
ENST00000611848.2:c.1295G=
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ENSP00000478613.2:p.Ser432=
|
|
ENST00000684953.1:n.2667G=
|
|
|
ENST00000685090.1:n.1746G=
|
|
|
ENST00000685232.1:n.1403G=
|
|
|
ENST00000688574.1:n.1403G=
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|
|
ENST00000691124.1:n.2777G=
|
|
|
ENST00000342988.8:c.1295G=
MANE Select
|
ENSP00000341551.3:p.Ser432=
|
|
ENST00000342988.7:c.1295G=
|
ENSP00000341551.3:p.Ser432=
|
|
ENST00000398417.6:c.1295G=
|
ENSP00000381452.1:p.Ser432=
|
|
ENST00000588745.5:c.1007G=
|
ENSP00000464901.1:p.Ser336=
|
|
ENST00000590499.1:n.353G=
|
|
|
ENST00000591126.5:n.3296G=
|
|
|
ENST00000592186.5:c.955+7258G=
|
ENSP00000468611.1:n.955+7258G=
|
|
ENST00000593223.1:c.62G=
|
ENSP00000466118.1:p.Ser21=
|
|
ENST00000611848.1:c.495G=
|
|
|
NM_005359.5:c.1295G= , LRG_318t1:c.1295G=
|
NP_005350.1:p.Ser432=
|
|
NM_005359.6:c.1295G=
MANE Select
|
NP_005350.1:p.Ser432=
|
|