ENST00000647720.2:c.3566G>T
|
ENSP00000497673.2:p.Ser1189Ile
|
|
ENST00000647978.2:c.*3480G>T
|
ENSP00000497658.1:n.*3480G>T
|
|
ENST00000649781.2:c.3583G>T
|
ENSP00000497203.1:p.Ala1195Ser
|
|
ENST00000685018.2:c.3766G>T
|
ENSP00000510194.2:p.Ala1256Ser
|
|
ENST00000687278.2:c.*419G>T
|
ENSP00000509593.2:n.*419G>T
|
|
ENST00000699585.1:c.3566G>T
|
ENSP00000514456.1:p.Ser1189Ile
|
|
ENST00000699598.1:c.3766G>T
|
ENSP00000514467.1:p.Ala1256Ser
|
|
ENST00000699599.1:c.3766G>T
|
ENSP00000514468.1:p.Ala1256Ser
|
|
ENST00000699600.1:c.*427G>T
|
ENSP00000514469.1:n.*427G>T
|
|
ENST00000699601.1:c.*2141G>T
|
ENSP00000514470.1:n.*2141G>T
|
|
ENST00000699602.1:c.3760G>T
|
ENSP00000514471.1:p.Ala1254Ser
|
|
ENST00000699604.1:c.*3590G>T
|
ENSP00000514472.1:n.*3590G>T
|
|
ENST00000699605.1:c.3340G>T
|
ENSP00000514473.1:p.Ala1114Ser
|
|
ENST00000685018.1:c.514G>T
|
ENSP00000510194.1:p.Ala172Ser
|
|
ENST00000687278.1:c.1553G>T
|
ENSP00000509593.1:n.1553G>T
|
|
ENST00000689011.1:c.348G>T
|
|
|
ENST00000003084.11:c.3766G>T
MANE Select
|
ENSP00000003084.6:p.Ala1256Ser
|
|
ENST00000647720.1:c.1216G>T
|
|
|
ENST00000649781.1:c.3583G>T
|
ENSP00000497203.1:p.Ala1195Ser
|
|
ENST00000003084.10:c.3766G>T
|
ENSP00000003084.6:p.Ala1256Ser
|
|
ENST00000426809.5:c.3676G>T
|
ENSP00000389119.1:p.Ala1226Ser
|
|
NM_000492.3:c.3766G>T , LRG_663t1:c.3766G>T
|
NP_000483.3:p.Ala1256Ser
|
|
XM_011515751.1:c.3856G>T
|
XP_011514053.1:p.Ala1286Ser
|
|
XM_011515752.1:c.3856G>T
|
XP_011514054.1:p.Ala1286Ser
|
|
XM_011515753.1:c.3523G>T
|
XP_011514055.1:p.Ala1175Ser
|
|
XM_011515754.1:c.3523G>T
|
XP_011514056.1:p.Ala1175Ser
|
|
NM_000492.4:c.3766G>T
MANE Select
|
NP_000483.3:p.Ala1256Ser
|
|