ENST00000647720.2:c.3587A>T
|
ENSP00000497673.2:p.His1196Leu
|
|
ENST00000647978.2:c.*3501A>T
|
ENSP00000497658.1:n.*3501A>T
|
|
ENST00000649781.2:c.3604A>T
|
ENSP00000497203.1:p.Thr1202Ser
|
|
ENST00000685018.2:c.3787A>T
|
ENSP00000510194.2:p.Thr1263Ser
|
|
ENST00000687278.2:c.*440A>T
|
ENSP00000509593.2:n.*440A>T
|
|
ENST00000699585.1:c.3587A>T
|
ENSP00000514456.1:p.His1196Leu
|
|
ENST00000699598.1:c.3787A>T
|
ENSP00000514467.1:p.Thr1263Ser
|
|
ENST00000699599.1:c.3787A>T
|
ENSP00000514468.1:p.Thr1263Ser
|
|
ENST00000699600.1:c.*448A>T
|
ENSP00000514469.1:n.*448A>T
|
|
ENST00000699601.1:c.*2162A>T
|
ENSP00000514470.1:n.*2162A>T
|
|
ENST00000699602.1:c.3781A>T
|
ENSP00000514471.1:p.Thr1261Ser
|
|
ENST00000699604.1:c.*3611A>T
|
ENSP00000514472.1:n.*3611A>T
|
|
ENST00000699605.1:c.3361A>T
|
ENSP00000514473.1:p.Thr1121Ser
|
|
ENST00000685018.1:c.535A>T
|
ENSP00000510194.1:p.Thr179Ser
|
|
ENST00000687278.1:c.1574A>T
|
ENSP00000509593.1:n.1574A>T
|
|
ENST00000689011.1:c.369A>T
|
|
|
ENST00000003084.11:c.3787A>T
MANE Select
|
ENSP00000003084.6:p.Thr1263Ser
|
|
ENST00000647720.1:c.1237A>T
|
|
|
ENST00000649781.1:c.3604A>T
|
ENSP00000497203.1:p.Thr1202Ser
|
|
ENST00000003084.10:c.3787A>T
|
ENSP00000003084.6:p.Thr1263Ser
|
|
ENST00000426809.5:c.3697A>T
|
ENSP00000389119.1:p.Thr1233Ser
|
|
NM_000492.3:c.3787A>T , LRG_663t1:c.3787A>T
|
NP_000483.3:p.Thr1263Ser
|
|
XM_011515751.1:c.3877A>T
|
XP_011514053.1:p.Thr1293Ser
|
|
XM_011515752.1:c.3877A>T
|
XP_011514054.1:p.Thr1293Ser
|
|
XM_011515753.1:c.3544A>T
|
XP_011514055.1:p.Thr1182Ser
|
|
XM_011515754.1:c.3544A>T
|
XP_011514056.1:p.Thr1182Ser
|
|
NM_000492.4:c.3787A>T
MANE Select
|
NP_000483.3:p.Thr1263Ser
|
|