ENST00000355832.10:c.2916C>G
MANE Select
|
ENSP00000348089.5:p.Ile972Met
|
|
ENST00000681632.1:n.4319C>G
|
|
|
ENST00000681659.1:c.2757C>G
|
ENSP00000505631.1:p.Ile919Met
|
|
ENST00000355832.9:c.2916C>G
|
ENSP00000348089.5:p.Ile972Met
|
|
ENST00000623073.3:c.*1212C>G
|
ENSP00000485650.1:n.*1212C>G
|
|
ENST00000623115.3:c.1026C>G
|
ENSP00000485321.1:p.Ile342Met
|
|
ENST00000624341.3:c.748C>G
|
|
|
NM_000124.3:c.2916C>G
|
NP_000115.1:p.Ile972Met
|
|
XR_945953.1:n.690-319G>C
|
|
|
NM_001346440.1:c.2916C>G
|
NP_001333369.1:p.Ile972Met
|
|
NM_000124.4:c.2916C>G
MANE Select
|
NP_000115.1:p.Ile972Met
|
|
NM_001346440.2:c.2916C>G
|
NP_001333369.1:p.Ile972Met
|
|