ENST00000682114.1:c.481T>C
|
ENSP00000507245.1:p.Tyr161His
|
|
ENST00000682478.1:n.671T>C
|
|
|
ENST00000683576.1:n.671T>C
|
|
|
ENST00000683627.1:c.481T>C
|
ENSP00000507533.1:p.Tyr161His
|
|
ENST00000684082.1:c.438T>C
|
ENSP00000508266.1:n.438T>C
|
|
ENST00000684633.1:n.453T>C
|
|
|
ENST00000684678.1:c.477T>C
|
ENSP00000507059.1:n.477T>C
|
|
ENST00000369842.9:c.481T>C
MANE Select
|
ENSP00000358857.4:p.Tyr161His
|
|
ENST00000369835.3:c.376T>C
|
ENSP00000358850.3:p.Tyr126His
|
|
ENST00000369842.8:c.481T>C
|
ENSP00000358857.4:p.Tyr161His
|
|
ENST00000428228.5:c.*386T>C
|
ENSP00000401081.1:n.*386T>C
|
|
ENST00000471965.1:n.270T>C
|
|
|
ENST00000485261.1:n.750T>C
|
|
|
ENST00000486738.5:n.918T>C
|
|
|
ENST00000492448.1:n.464T>C
|
|
|
NM_000117.2:c.481T>C , LRG_745t1:c.481T>C
|
NP_000108.1:p.Tyr161His
|
|
XM_024452349.1:c.487T>C
|
XP_024308117.1:p.Tyr163His
|
|
NM_000117.3:c.481T>C
MANE Select
|
NP_000108.1:p.Tyr161His
|
|