ENST00000355832.10:c.3418A>G
MANE Select
|
ENSP00000348089.5:p.Met1140Val
|
|
ENST00000679552.1:n.489A>G
|
|
|
ENST00000679871.1:n.564A>G
|
|
|
ENST00000679974.1:n.467A>G
|
|
|
ENST00000681632.1:n.4821A>G
|
|
|
ENST00000681659.1:c.3259A>G
|
ENSP00000505631.1:p.Met1087Val
|
|
ENST00000355832.9:c.3418A>G
|
ENSP00000348089.5:p.Met1140Val
|
|
ENST00000623073.3:c.*1714A>G
|
ENSP00000485650.1:n.*1714A>G
|
|
ENST00000623115.3:c.1528A>G
|
ENSP00000485321.1:p.Met510Val
|
|
ENST00000624341.3:c.1250A>G
|
|
|
NM_000124.3:c.3418A>G
|
NP_000115.1:p.Met1140Val
|
|
XR_945953.1:n.243-1023T>C
|
|
|
NM_001346440.1:c.3418A>G
|
NP_001333369.1:p.Met1140Val
|
|
NM_000124.4:c.3418A>G
MANE Select
|
NP_000115.1:p.Met1140Val
|
|
NM_001346440.2:c.3418A>G
|
NP_001333369.1:p.Met1140Val
|
|