ENST00000393716.8:c.335T=
MANE Select
|
ENSP00000377319.3:p.Ile112=
|
|
ENST00000466380.6:c.335T=
|
ENSP00000420297.2:p.Ile112=
|
|
ENST00000337940.4:c.452T=
|
ENSP00000336528.4:p.Ile151=
|
|
ENST00000393716.6:c.335T=
|
ENSP00000377319.2:p.Ile112=
|
|
ENST00000466380.5:c.335T=
|
ENSP00000420297.1:p.Ile112=
|
|
ENST00000493757.1:n.467T=
|
|
|
NM_003889.3:c.335T=
|
NP_003880.3:p.Ile112=
|
|
NM_022002.2:c.452T=
|
NP_071285.1:p.Ile151=
|
|
NM_033013.2:c.335T=
|
NP_148934.1:p.Ile112=
|
|
NM_003889.4:c.335T=
MANE Select
|
NP_003880.3:p.Ile112=
|
|
NM_022002.3:c.452T=
|
NP_071285.1:p.Ile151=
|
|
NM_033013.3:c.335T=
|
NP_148934.1:p.Ile112=
|
|