ENST00000682114.1:c.396C>T
|
ENSP00000507245.1:p.His132=
|
|
ENST00000682478.1:n.586C>T
|
|
|
ENST00000683576.1:n.586C>T
|
|
|
ENST00000683627.1:c.396C>T
|
ENSP00000507533.1:p.His132=
|
|
ENST00000684082.1:c.353C>T
|
ENSP00000508266.1:n.353C>T
|
|
ENST00000684633.1:n.368C>T
|
|
|
ENST00000684678.1:c.392C>T
|
ENSP00000507059.1:n.392C>T
|
|
ENST00000369842.9:c.396C>T
MANE Select
|
ENSP00000358857.4:p.His132=
|
|
ENST00000369835.3:c.291C>T
|
ENSP00000358850.3:p.His97=
|
|
ENST00000369842.8:c.396C>T
|
ENSP00000358857.4:p.His132=
|
|
ENST00000428228.5:c.*301C>T
|
ENSP00000401081.1:n.*301C>T
|
|
ENST00000468294.5:n.356C>T
|
|
|
ENST00000485261.1:n.586C>T
|
|
|
ENST00000486738.5:n.754C>T
|
|
|
ENST00000492448.1:n.379C>T
|
|
|
ENST00000494443.5:n.667C>T
|
|
|
NM_000117.2:c.396C>T , LRG_745t1:c.396C>T
|
NP_000108.1:p.His132=
|
|
XM_024452349.1:c.402C>T
|
XP_024308117.1:p.His134=
|
|
NM_000117.3:c.396C>T
MANE Select
|
NP_000108.1:p.His132=
|
|