ENST00000355832.10:c.3899C>T
MANE Select
|
ENSP00000348089.5:p.Ser1300Phe
|
|
ENST00000679552.1:n.970C>T
|
|
|
ENST00000679871.1:n.1045C>T
|
|
|
ENST00000679974.1:n.948C>T
|
|
|
ENST00000681632.1:n.5302C>T
|
|
|
ENST00000681659.1:c.3740C>T
|
ENSP00000505631.1:p.Ser1247Phe
|
|
ENST00000355832.9:c.3899C>T
|
ENSP00000348089.5:p.Ser1300Phe
|
|
ENST00000465653.1:n.221C>T
|
|
|
ENST00000623073.3:c.*2195C>T
|
ENSP00000485650.1:n.*2195C>T
|
|
ENST00000623115.3:c.2009C>T
|
ENSP00000485321.1:p.Ser670Phe
|
|
ENST00000624341.3:c.1731C>T
|
|
|
NM_000124.3:c.3899C>T
|
NP_000115.1:p.Ser1300Phe
|
|
XR_945953.1:n.243-10129G>A
|
|
|
NM_001346440.1:c.3899C>T
|
NP_001333369.1:p.Ser1300Phe
|
|
NM_000124.4:c.3899C>T
MANE Select
|
NP_000115.1:p.Ser1300Phe
|
|
NM_001346440.2:c.3899C>T
|
NP_001333369.1:p.Ser1300Phe
|
|