ENST00000355832.10:c.3358T>C
MANE Select
|
ENSP00000348089.5:p.Leu1120=
|
|
ENST00000679552.1:n.429T>C
|
|
|
ENST00000679871.1:n.504T>C
|
|
|
ENST00000679974.1:n.407T>C
|
|
|
ENST00000681632.1:n.4761T>C
|
|
|
ENST00000681659.1:c.3199T>C
|
ENSP00000505631.1:p.Leu1067=
|
|
ENST00000355832.9:c.3358T>C
|
ENSP00000348089.5:p.Leu1120=
|
|
ENST00000623073.3:c.*1654T>C
|
ENSP00000485650.1:n.*1654T>C
|
|
ENST00000623115.3:c.1468T>C
|
ENSP00000485321.1:p.Leu490=
|
|
ENST00000624341.3:c.1190T>C
|
|
|
NM_000124.3:c.3358T>C
|
NP_000115.1:p.Leu1120=
|
|
XR_945953.1:n.243-963A>G
|
|
|
NM_001346440.1:c.3358T>C
|
NP_001333369.1:p.Leu1120=
|
|
NM_000124.4:c.3358T>C
MANE Select
|
NP_000115.1:p.Leu1120=
|
|
NM_001346440.2:c.3358T>C
|
NP_001333369.1:p.Leu1120=
|
|