ENST00000647720.2:c.*62G>T
|
ENSP00000497673.2:n.*62G>T
|
|
ENST00000647978.2:c.*3567G>T
|
ENSP00000497658.1:n.*3567G>T
|
|
ENST00000649781.2:c.3670G>T
|
ENSP00000497203.1:p.Ala1224Ser
|
|
ENST00000685018.2:c.3853G>T
|
ENSP00000510194.2:p.Ala1285Ser
|
|
ENST00000687278.2:c.*506G>T
|
ENSP00000509593.2:n.*506G>T
|
|
ENST00000699585.1:c.*62G>T
|
ENSP00000514456.1:n.*62G>T
|
|
ENST00000699598.1:c.3853G>T
|
ENSP00000514467.1:p.Ala1285Ser
|
|
ENST00000699599.1:c.3853G>T
|
ENSP00000514468.1:p.Ala1285Ser
|
|
ENST00000699600.1:c.*514G>T
|
ENSP00000514469.1:n.*514G>T
|
|
ENST00000699601.1:c.*2228G>T
|
ENSP00000514470.1:n.*2228G>T
|
|
ENST00000699602.1:c.3847G>T
|
ENSP00000514471.1:p.Ala1283Ser
|
|
ENST00000699604.1:c.*3677G>T
|
ENSP00000514472.1:n.*3677G>T
|
|
ENST00000699605.1:c.3427G>T
|
ENSP00000514473.1:p.Ala1143Ser
|
|
ENST00000685018.1:c.601G>T
|
ENSP00000510194.1:p.Ala201Ser
|
|
ENST00000687278.1:c.1640G>T
|
ENSP00000509593.1:n.1640G>T
|
|
ENST00000689011.1:c.435G>T
|
|
|
ENST00000003084.11:c.3853G>T
MANE Select
|
ENSP00000003084.6:p.Ala1285Ser
|
|
ENST00000647720.1:c.1303G>T
|
|
|
ENST00000649781.1:c.3670G>T
|
ENSP00000497203.1:p.Ala1224Ser
|
|
ENST00000003084.10:c.3853G>T
|
ENSP00000003084.6:p.Ala1285Ser
|
|
ENST00000426809.5:c.3763G>T
|
ENSP00000389119.1:p.Ala1255Ser
|
|
NM_000492.3:c.3853G>T , LRG_663t1:c.3853G>T
|
NP_000483.3:p.Ala1285Ser
|
|
XM_011515751.1:c.3943G>T
|
XP_011514053.1:p.Ala1315Ser
|
|
XM_011515752.1:c.3943G>T
|
XP_011514054.1:p.Ala1315Ser
|
|
XM_011515753.1:c.3610G>T
|
XP_011514055.1:p.Ala1204Ser
|
|
XM_011515754.1:c.3610G>T
|
XP_011514056.1:p.Ala1204Ser
|
|
NM_000492.4:c.3853G>T
MANE Select
|
NP_000483.3:p.Ala1285Ser
|
|