ENST00000374467.4:c.297C>T
(BAK1)
MANE Select
|
ENSP00000363591.3:p.His99=
|
|
ENST00000360661.9:c.237C>T
(BAK1)
|
ENSP00000353878.6:p.His79=
|
|
ENST00000374467.3:c.297C>T
(BAK1)
|
ENSP00000363591.3:p.His99=
|
|
ENST00000442998.6:c.297C>T
(BAK1)
|
ENSP00000391258.2:p.His99=
|
|
ENST00000612409.1:n.249G>A
(GGNBP1)
|
|
|
NM_001188.3:c.297C>T
(BAK1)
|
NP_001179.1:p.His99=
|
|
XM_011514779.1:c.297C>T
(BAK1)
|
XP_011513081.1:p.His99=
|
|
XM_011514780.1:c.120C>T
(BAK1)
|
XP_011513082.1:p.His40=
|
|
XM_011514779.3:c.297C>T
(BAK1)
|
XP_011513081.1:p.His99=
|
|
NM_001188.4:c.297C>T
(BAK1)
MANE Select
|
NP_001179.1:p.His99=
|
|