ENST00000355832.10:c.2929A>G
MANE Select
|
ENSP00000348089.5:p.Ile977Val
|
|
ENST00000679552.1:n.142-227A>G
|
|
|
ENST00000679871.1:n.75A>G
|
|
|
ENST00000679974.1:n.120-227A>G
|
|
|
ENST00000681632.1:n.4332A>G
|
|
|
ENST00000681659.1:c.2770A>G
|
ENSP00000505631.1:p.Ile924Val
|
|
ENST00000355832.9:c.2929A>G
|
ENSP00000348089.5:p.Ile977Val
|
|
ENST00000623073.3:c.*1225A>G
|
ENSP00000485650.1:n.*1225A>G
|
|
ENST00000623115.3:c.1039A>G
|
ENSP00000485321.1:p.Ile347Val
|
|
ENST00000624341.3:c.761A>G
|
|
|
NM_000124.3:c.2929A>G
|
NP_000115.1:p.Ile977Val
|
|
XR_945953.1:n.243-449T>C
|
|
|
NM_001346440.1:c.2929A>G
|
NP_001333369.1:p.Ile977Val
|
|
NM_000124.4:c.2929A>G
MANE Select
|
NP_000115.1:p.Ile977Val
|
|
NM_001346440.2:c.2929A>G
|
NP_001333369.1:p.Ile977Val
|
|