ENST00000355832.10:c.3901C>G
MANE Select
|
ENSP00000348089.5:p.Arg1301Gly
|
|
ENST00000679552.1:n.972C>G
|
|
|
ENST00000679871.1:n.1047C>G
|
|
|
ENST00000679974.1:n.950C>G
|
|
|
ENST00000681632.1:n.5304C>G
|
|
|
ENST00000681659.1:c.3742C>G
|
ENSP00000505631.1:p.Arg1248Gly
|
|
ENST00000355832.9:c.3901C>G
|
ENSP00000348089.5:p.Arg1301Gly
|
|
ENST00000465653.1:n.223C>G
|
|
|
ENST00000623073.3:c.*2197C>G
|
ENSP00000485650.1:n.*2197C>G
|
|
ENST00000623115.3:c.2011C>G
|
ENSP00000485321.1:p.Arg671Gly
|
|
ENST00000624341.3:c.1733C>G
|
|
|
NM_000124.3:c.3901C>G
|
NP_000115.1:p.Arg1301Gly
|
|
XR_945953.1:n.243-10131G>C
|
|
|
NM_001346440.1:c.3901C>G
|
NP_001333369.1:p.Arg1301Gly
|
|
NM_000124.4:c.3901C>G
MANE Select
|
NP_000115.1:p.Arg1301Gly
|
|
NM_001346440.2:c.3901C>G
|
NP_001333369.1:p.Arg1301Gly
|
|