ENST00000682114.1:c.496C>T
|
ENSP00000507245.1:p.His166Tyr
|
|
ENST00000682478.1:n.686C>T
|
|
|
ENST00000683576.1:n.686C>T
|
|
|
ENST00000683627.1:c.496C>T
|
ENSP00000507533.1:p.His166Tyr
|
|
ENST00000684082.1:c.453C>T
|
ENSP00000508266.1:n.453C>T
|
|
ENST00000684633.1:n.468C>T
|
|
|
ENST00000684678.1:c.492C>T
|
ENSP00000507059.1:n.492C>T
|
|
ENST00000369842.9:c.496C>T
MANE Select
|
ENSP00000358857.4:p.His166Tyr
|
|
ENST00000369835.3:c.391C>T
|
ENSP00000358850.3:p.His131Tyr
|
|
ENST00000369842.8:c.496C>T
|
ENSP00000358857.4:p.His166Tyr
|
|
ENST00000428228.5:c.*401C>T
|
ENSP00000401081.1:n.*401C>T
|
|
ENST00000471965.1:n.285C>T
|
|
|
ENST00000485261.1:n.765C>T
|
|
|
ENST00000486738.5:n.933C>T
|
|
|
ENST00000492448.1:n.479C>T
|
|
|
NM_000117.2:c.496C>T , LRG_745t1:c.496C>T
|
NP_000108.1:p.His166Tyr
|
|
XM_024452349.1:c.502C>T
|
XP_024308117.1:p.His168Tyr
|
|
NM_000117.3:c.496C>T
MANE Select
|
NP_000108.1:p.His166Tyr
|
|