ENST00000650516.2:c.864T>C
|
ENSP00000498052.2:p.Phe288=
|
|
ENST00000343257.7:c.864T>C
MANE Select
|
ENSP00000339867.2:p.Phe288=
|
|
ENST00000432192.6:c.688T>C
|
|
|
ENST00000455478.6:c.452T>C
|
ENSP00000400027.2:n.452T>C
|
|
ENST00000650516.1:c.864T>C
|
ENSP00000498052.1:p.Phe288=
|
|
ENST00000343257.6:c.864T>C
|
ENSP00000339867.2:p.Phe288=
|
|
ENST00000432192.5:c.378T>C
|
|
|
ENST00000455478.5:c.456T>C
|
|
|
ENST00000495612.1:n.165T>C
|
|
|
NM_000083.2:c.864T>C
|
NP_000074.2:p.Phe288=
|
|
NR_046453.1:n.954T>C
|
|
|
XM_011515781.1:c.864T>C
|
XP_011514083.1:p.Phe288=
|
|
XM_017011739.1:c.414T>C
|
XP_016867228.1:p.Phe138=
|
|
XM_017011740.1:c.414T>C
|
XP_016867229.1:p.Phe138=
|
|
NM_000083.3:c.864T>C
MANE Select
|
NP_000074.3:p.Phe288=
|
|
NR_046453.2:n.969T>C
|
|
|