ENST00000311604.8:c.987G>A
MANE Select
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ENSP00000308383.4:p.Glu329=
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ENST00000311604.7:c.987G>A
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ENSP00000308383.3:p.Glu329=
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ENST00000381775.5:c.1371G>A
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ENSP00000371194.1:p.Glu457=
|
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ENST00000405957.6:c.801G>A
|
ENSP00000383932.2:p.Glu267=
|
|
ENST00000406638.6:c.801G>A
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ENSP00000384022.2:p.Glu267=
|
|
ENST00000472974.5:n.857G>A
|
|
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ENST00000485341.5:n.1483G>A
|
|
|
ENST00000612798.4:c.801G>A
|
ENSP00000484140.1:p.Glu267=
|
|
NM_001013253.1:c.801G>A
|
NP_001013271.1:p.Glu267=
|
|
NM_001013254.1:c.801G>A
|
NP_001013272.1:p.Glu267=
|
|
NM_001013255.1:c.801G>A
|
NP_001013273.1:p.Glu267=
|
|
NM_001242932.1:c.1371G>A
|
NP_001229861.1:p.Glu457=
|
|
NM_001289005.1:c.801G>A
|
NP_001275934.1:p.Glu267=
|
|
NM_002339.2:c.987G>A
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NP_002330.1:p.Glu329=
|
|
NM_001013253.2:c.801G>A
|
NP_001013271.1:p.Glu267=
|
|
NM_002339.3:c.987G>A
MANE Select
|
NP_002330.1:p.Glu329=
|
|
NM_001242932.2:c.1371G>A
|
NP_001229861.1:p.Glu457=
|
|
NM_001289005.2:c.801G>A
|
NP_001275934.1:p.Glu267=
|
|