ENST00000490576.2:c.-1-228G>T
|
ENSP00000478839.2:n.-1-228G>T
|
|
ENST00000610745.5:c.-2+163G>T
MANE Select
|
ENSP00000478561.1:n.-2+163G>T
|
|
ENST00000490576.1:c.-1-228G>T
|
ENSP00000478839.1:n.-1-228G>T
|
|
ENST00000494864.1:c.-70-4307G>T
|
ENSP00000479876.1:n.-70-4307G>T
|
|
ENST00000610745.4:c.-2+163G>T
|
ENSP00000478561.1:n.-2+163G>T
|
|
ENST00000613082.1:n.375+163G>T
|
|
|
ENST00000614273.1:c.-2+159G>T
|
ENSP00000483678.1:n.-2+159G>T
|
|
NM_000104.3:c.-2+163G>T
|
NP_000095.2:n.-2+163G>T
|
|
XM_011533236.1:c.231C>A
|
XP_011531538.1:p.Ser77=
|
|
NM_000104.4:c.-2+163G>T
MANE Select
|
NP_000095.2:n.-2+163G>T
|
|