ENST00000682114.1:c.463T>C
|
ENSP00000507245.1:p.Tyr155His
|
|
ENST00000682478.1:n.653T>C
|
|
|
ENST00000683576.1:n.653T>C
|
|
|
ENST00000683627.1:c.463T>C
|
ENSP00000507533.1:p.Tyr155His
|
|
ENST00000684082.1:c.420T>C
|
ENSP00000508266.1:n.420T>C
|
|
ENST00000684633.1:n.435T>C
|
|
|
ENST00000684678.1:c.459T>C
|
ENSP00000507059.1:n.459T>C
|
|
ENST00000369842.9:c.463T>C
MANE Select
|
ENSP00000358857.4:p.Tyr155His
|
|
ENST00000369835.3:c.358T>C
|
ENSP00000358850.3:p.Tyr120His
|
|
ENST00000369842.8:c.463T>C
|
ENSP00000358857.4:p.Tyr155His
|
|
ENST00000428228.5:c.*368T>C
|
ENSP00000401081.1:n.*368T>C
|
|
ENST00000471965.1:n.252T>C
|
|
|
ENST00000485261.1:n.732T>C
|
|
|
ENST00000486738.5:n.900T>C
|
|
|
ENST00000492448.1:n.446T>C
|
|
|
NM_000117.2:c.463T>C , LRG_745t1:c.463T>C
|
NP_000108.1:p.Tyr155His
|
|
XM_024452349.1:c.469T>C
|
XP_024308117.1:p.Tyr157His
|
|
NM_000117.3:c.463T>C
MANE Select
|
NP_000108.1:p.Tyr155His
|
|