ENST00000650516.2:c.1729_1732del
|
ENSP00000498052.2:p.Leu577MetfsTer?
|
|
ENST00000343257.7:c.1729_1732del
MANE Select
|
ENSP00000339867.2:p.Leu577MetfsTer?
|
|
ENST00000432192.6:c.1553_1556del
|
|
|
ENST00000343257.6:c.1729_1732del
|
ENSP00000339867.2:p.Leu577MetfsTer?
|
|
NM_000083.2:c.1729_1732del
|
NP_000074.2:p.Leu577MetfsTer?
|
|
NR_046453.1:n.1669_1672del
|
|
|
XM_011515781.1:c.1753_1756del
|
XP_011514083.1:p.Leu585MetfsTer?
|
|
XM_011515782.1:c.475_478del
|
XP_011514084.1:p.Leu159MetfsTer?
|
|
XM_011515782.2:c.475_478del
|
XP_011514084.1:p.Leu159MetfsTer?
|
|
XM_017011739.1:c.1303_1306del
|
XP_016867228.1:p.Leu435MetfsTer?
|
|
XM_017011740.1:c.1279_1282del
|
XP_016867229.1:p.Leu427MetfsTer?
|
|
NM_000083.3:c.1729_1732del
MANE Select
|
NP_000074.3:p.Leu577MetfsTer?
|
|
NR_046453.2:n.1684_1687del
|
|
|