ENST00000647720.2:c.2943A>T
|
ENSP00000497673.2:p.Ala981=
|
|
ENST00000647978.2:c.*2657A>T
|
ENSP00000497658.1:n.*2657A>T
|
|
ENST00000649781.2:c.2760A>T
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ENSP00000497203.1:p.Ala920=
|
|
ENST00000685018.2:c.2943A>T
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ENSP00000510194.2:p.Ala981=
|
|
ENST00000687278.2:c.2943A>T
|
ENSP00000509593.2:p.Ala981=
|
|
ENST00000699585.1:c.2943A>T
|
ENSP00000514456.1:p.Ala981=
|
|
ENST00000699598.1:c.2943A>T
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ENSP00000514467.1:p.Ala981=
|
|
ENST00000699599.1:c.2943A>T
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ENSP00000514468.1:p.Ala981=
|
|
ENST00000699600.1:c.2943A>T
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ENSP00000514469.1:p.Ala981=
|
|
ENST00000699601.1:c.*1243A>T
|
ENSP00000514470.1:n.*1243A>T
|
|
ENST00000699602.1:c.2943A>T
|
ENSP00000514471.1:p.Ala981=
|
|
ENST00000699604.1:c.*2767A>T
|
ENSP00000514472.1:n.*2767A>T
|
|
ENST00000699605.1:c.2517A>T
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ENSP00000514473.1:p.Ala839=
|
|
ENST00000687278.1:c.534A>T
|
ENSP00000509593.1:p.Ala178=
|
|
ENST00000003084.11:c.2943A>T
MANE Select
|
ENSP00000003084.6:p.Ala981=
|
|
ENST00000647720.1:c.593A>T
|
|
|
ENST00000648260.1:c.1725A>T
|
ENSP00000497957.1:p.Ala575=
|
|
ENST00000649406.1:c.2760A>T
|
ENSP00000497965.1:p.Ala920=
|
|
ENST00000649781.1:c.2760A>T
|
ENSP00000497203.1:p.Ala920=
|
|
ENST00000003084.10:c.2943A>T
|
ENSP00000003084.6:p.Ala981=
|
|
ENST00000426809.5:c.2853A>T
|
ENSP00000389119.1:p.Ala951=
|
|
NM_000492.3:c.2943A>T , LRG_663t1:c.2943A>T
|
NP_000483.3:p.Ala981=
|
|
XM_011515751.1:c.3033A>T
|
XP_011514053.1:p.Ala1011=
|
|
XM_011515752.1:c.3033A>T
|
XP_011514054.1:p.Ala1011=
|
|
XM_011515753.1:c.2700A>T
|
XP_011514055.1:p.Ala900=
|
|
XM_011515754.1:c.2700A>T
|
XP_011514056.1:p.Ala900=
|
|
NM_000492.4:c.2943A>T
MANE Select
|
NP_000483.3:p.Ala981=
|
|