ENST00000355832.10:c.2032A>G
MANE Select
|
ENSP00000348089.5:p.Met678Val
|
|
ENST00000681632.1:n.2110A>G
|
|
|
ENST00000681659.1:c.1873A>G
|
ENSP00000505631.1:p.Met625Val
|
|
ENST00000355832.9:c.2032A>G
|
ENSP00000348089.5:p.Met678Val
|
|
ENST00000623073.3:c.*424A>G
|
ENSP00000485650.1:n.*424A>G
|
|
ENST00000623115.3:c.142A>G
|
ENSP00000485321.1:p.Met48Val
|
|
NM_000124.3:c.2032A>G
|
NP_000115.1:p.Met678Val
|
|
NM_001346440.1:c.2032A>G
|
NP_001333369.1:p.Met678Val
|
|
NM_000124.4:c.2032A>G
MANE Select
|
NP_000115.1:p.Met678Val
|
|
NM_001346440.2:c.2032A>G
|
NP_001333369.1:p.Met678Val
|
|