ENST00000647720.2:c.3589T>A
|
ENSP00000497673.2:p.Ter1197Arg
|
|
ENST00000647978.2:c.*3503T>A
|
ENSP00000497658.1:n.*3503T>A
|
|
ENST00000649781.2:c.3606T>A
|
ENSP00000497203.1:p.Thr1202=
|
|
ENST00000685018.2:c.3789T>A
|
ENSP00000510194.2:p.Thr1263=
|
|
ENST00000687278.2:c.*442T>A
|
ENSP00000509593.2:n.*442T>A
|
|
ENST00000699585.1:c.3589T>A
|
ENSP00000514456.1:p.Ter1197Arg
|
|
ENST00000699598.1:c.3789T>A
|
ENSP00000514467.1:p.Thr1263=
|
|
ENST00000699599.1:c.3789T>A
|
ENSP00000514468.1:p.Thr1263=
|
|
ENST00000699600.1:c.*450T>A
|
ENSP00000514469.1:n.*450T>A
|
|
ENST00000699601.1:c.*2164T>A
|
ENSP00000514470.1:n.*2164T>A
|
|
ENST00000699602.1:c.3783T>A
|
ENSP00000514471.1:p.Thr1261=
|
|
ENST00000699604.1:c.*3613T>A
|
ENSP00000514472.1:n.*3613T>A
|
|
ENST00000699605.1:c.3363T>A
|
ENSP00000514473.1:p.Thr1121=
|
|
ENST00000685018.1:c.537T>A
|
ENSP00000510194.1:p.Thr179=
|
|
ENST00000687278.1:c.1576T>A
|
ENSP00000509593.1:n.1576T>A
|
|
ENST00000689011.1:c.371T>A
|
|
|
ENST00000003084.11:c.3789T>A
MANE Select
|
ENSP00000003084.6:p.Thr1263=
|
|
ENST00000647720.1:c.1239T>A
|
|
|
ENST00000649781.1:c.3606T>A
|
ENSP00000497203.1:p.Thr1202=
|
|
ENST00000003084.10:c.3789T>A
|
ENSP00000003084.6:p.Thr1263=
|
|
ENST00000426809.5:c.3699T>A
|
ENSP00000389119.1:p.Thr1233=
|
|
NM_000492.3:c.3789T>A , LRG_663t1:c.3789T>A
|
NP_000483.3:p.Thr1263=
|
|
XM_011515751.1:c.3879T>A
|
XP_011514053.1:p.Thr1293=
|
|
XM_011515752.1:c.3879T>A
|
XP_011514054.1:p.Thr1293=
|
|
XM_011515753.1:c.3546T>A
|
XP_011514055.1:p.Thr1182=
|
|
XM_011515754.1:c.3546T>A
|
XP_011514056.1:p.Thr1182=
|
|
NM_000492.4:c.3789T>A
MANE Select
|
NP_000483.3:p.Thr1263=
|
|