|
ENST00000647720.2:c.2863T>G
|
ENSP00000497673.2:p.Ser955Ala
|
|
|
ENST00000647978.2:c.*2577T>G
|
ENSP00000497658.1:n.*2577T>G
|
|
|
ENST00000649781.2:c.2680T>G
|
ENSP00000497203.1:p.Ser894Ala
|
|
|
ENST00000685018.2:c.2863T>G
|
ENSP00000510194.2:p.Ser955Ala
|
|
|
ENST00000687278.2:c.2863T>G
|
ENSP00000509593.2:p.Ser955Ala
|
|
|
ENST00000699585.1:c.2863T>G
|
ENSP00000514456.1:p.Ser955Ala
|
|
|
ENST00000699598.1:c.2863T>G
|
ENSP00000514467.1:p.Ser955Ala
|
|
|
ENST00000699599.1:c.2863T>G
|
ENSP00000514468.1:p.Ser955Ala
|
|
|
ENST00000699600.1:c.2863T>G
|
ENSP00000514469.1:p.Ser955Ala
|
|
|
ENST00000699601.1:c.*1163T>G
|
ENSP00000514470.1:n.*1163T>G
|
|
|
ENST00000699602.1:c.2863T>G
|
ENSP00000514471.1:p.Ser955Ala
|
|
|
ENST00000699604.1:c.*2687T>G
|
ENSP00000514472.1:n.*2687T>G
|
|
|
ENST00000699605.1:c.2437T>G
|
ENSP00000514473.1:p.Ser813Ala
|
|
|
ENST00000687278.1:c.454T>G
|
ENSP00000509593.1:p.Ser152Ala
|
|
|
ENST00000003084.11:c.2863T>G
MANE Select
|
ENSP00000003084.6:p.Ser955Ala
|
|
|
ENST00000647720.1:c.513T>G
|
|
|
|
ENST00000648260.1:c.1645T>G
|
ENSP00000497957.1:p.Ser549Ala
|
|
|
ENST00000649406.1:c.2680T>G
|
ENSP00000497965.1:p.Ser894Ala
|
|
|
ENST00000649781.1:c.2680T>G
|
ENSP00000497203.1:p.Ser894Ala
|
|
|
ENST00000003084.10:c.2863T>G
|
ENSP00000003084.6:p.Ser955Ala
|
|
|
ENST00000426809.5:c.2773T>G
|
ENSP00000389119.1:p.Ser925Ala
|
|
|
NM_000492.3:c.2863T>G , LRG_663t1:c.2863T>G
|
NP_000483.3:p.Ser955Ala
|
|
|
XM_011515751.1:c.2953T>G
|
XP_011514053.1:p.Ser985Ala
|
|
|
XM_011515752.1:c.2953T>G
|
XP_011514054.1:p.Ser985Ala
|
|
|
XM_011515753.1:c.2620T>G
|
XP_011514055.1:p.Ser874Ala
|
|
|
XM_011515754.1:c.2620T>G
|
XP_011514056.1:p.Ser874Ala
|
|
|
NM_000492.4:c.2863T>G
MANE Select
|
NP_000483.3:p.Ser955Ala
|
|
