ENST00000470094.2:c.*589T>A
|
ENSP00000434898.2:n.*589T>A
|
|
ENST00000528762.2:c.*1433T>A
|
ENSP00000433168.2:n.*1433T>A
|
|
ENST00000530893.7:c.9697T>A
|
ENSP00000499438.2:p.Ser3233Thr
|
|
ENST00000665585.2:c.*1628T>A
|
ENSP00000499570.2:n.*1628T>A
|
|
ENST00000700202.2:c.10015T>A
|
ENSP00000514856.2:p.Ser3339Thr
|
|
ENST00000700202.1:c.2482T>A
|
ENSP00000514856.1:p.Ser828Thr
|
|
ENST00000700203.1:n.2193T>A
|
|
|
ENST00000380152.8:c.10066T>A
MANE Select
|
ENSP00000369497.3:p.Ser3356Thr
|
|
ENST00000544455.6:c.10066T>A
|
ENSP00000439902.1:p.Ser3356Thr
|
|
ENST00000614259.2:c.10074T>A
|
ENSP00000506251.1:n.10074T>A
|
|
ENST00000680887.1:c.10066T>A
|
ENSP00000505508.1:p.Ser3356Thr
|
|
ENST00000380152.7:c.10066T>A
|
ENSP00000369497.3:p.Ser3356Thr
|
|
ENST00000544455.5:c.10066T>A
|
ENSP00000439902.1:p.Ser3356Thr
|
|
NM_000059.3:c.10066T>A , LRG_293t1:c.10066T>A
|
NP_000050.2:p.Ser3356Thr
|
|
XM_011535203.1:c.10066T>A
|
XP_011533505.1:p.Ser3356Thr
|
|
XM_011535204.1:c.9970T>A
|
XP_011533506.1:p.Ser3324Thr
|
|
NM_000059.4:c.10066T>A
MANE Select
|
NP_000050.3:p.Ser3356Thr
|
|