ENST00000355832.10:c.3003C>G
MANE Select
|
ENSP00000348089.5:p.Leu1001=
|
|
ENST00000679552.1:n.142-153C>G
|
|
|
ENST00000679871.1:n.149C>G
|
|
|
ENST00000679974.1:n.120-153C>G
|
|
|
ENST00000681632.1:n.4406C>G
|
|
|
ENST00000681659.1:c.2844C>G
|
ENSP00000505631.1:p.Leu948=
|
|
ENST00000355832.9:c.3003C>G
|
ENSP00000348089.5:p.Leu1001=
|
|
ENST00000623073.3:c.*1299C>G
|
ENSP00000485650.1:n.*1299C>G
|
|
ENST00000623115.3:c.1113C>G
|
ENSP00000485321.1:p.Leu371=
|
|
ENST00000624341.3:c.835C>G
|
|
|
NM_000124.3:c.3003C>G
|
NP_000115.1:p.Leu1001=
|
|
XR_945953.1:n.243-523G>C
|
|
|
NM_001346440.1:c.3003C>G
|
NP_001333369.1:p.Leu1001=
|
|
NM_000124.4:c.3003C>G
MANE Select
|
NP_000115.1:p.Leu1001=
|
|
NM_001346440.2:c.3003C>G
|
NP_001333369.1:p.Leu1001=
|
|