ENST00000682114.1:c.556T>A
|
ENSP00000507245.1:p.Ser186Thr
|
|
ENST00000682478.1:n.746T>A
|
|
|
ENST00000683576.1:n.746T>A
|
|
|
ENST00000683627.1:c.556T>A
|
ENSP00000507533.1:p.Ser186Thr
|
|
ENST00000684082.1:c.513T>A
|
ENSP00000508266.1:n.513T>A
|
|
ENST00000684633.1:n.528T>A
|
|
|
ENST00000684678.1:c.552T>A
|
ENSP00000507059.1:n.552T>A
|
|
ENST00000369842.9:c.556T>A
MANE Select
|
ENSP00000358857.4:p.Ser186Thr
|
|
ENST00000369835.3:c.451T>A
|
ENSP00000358850.3:p.Ser151Thr
|
|
ENST00000369842.8:c.556T>A
|
ENSP00000358857.4:p.Ser186Thr
|
|
ENST00000428228.5:c.*461T>A
|
ENSP00000401081.1:n.*461T>A
|
|
ENST00000471965.1:n.345T>A
|
|
|
ENST00000486738.5:n.993T>A
|
|
|
ENST00000492448.1:n.539T>A
|
|
|
NM_000117.2:c.556T>A , LRG_745t1:c.556T>A
|
NP_000108.1:p.Ser186Thr
|
|
XM_024452349.1:c.562T>A
|
XP_024308117.1:p.Ser188Thr
|
|
NM_000117.3:c.556T>A
MANE Select
|
NP_000108.1:p.Ser186Thr
|
|