ENST00000553645.7:c.*200C>G
MANE Select
|
ENSP00000452037.1:n.*200C>G
|
|
ENST00000311089.7:c.*200C>G
|
ENSP00000310360.3:n.*200C>G
|
|
ENST00000553645.6:c.*200C>G
|
ENSP00000452037.1:n.*200C>G
|
|
ENST00000554339.5:c.*200C>G
|
ENSP00000450744.1:n.*200C>G
|
|
NM_001201366.1:c.*200C>G
|
NP_001188295.1:n.*200C>G
|
|
NM_031427.3:c.*200C>G
|
NP_113615.2:n.*200C>G
|
|
XM_017021679.2:c.*200C>G
|
XP_016877168.1:n.*200C>G
|
|
XM_024449715.1:c.*200C>G
|
XP_024305483.1:n.*200C>G
|
|
NM_031427.4:c.*200C>G
MANE Select
|
NP_113615.2:n.*200C>G
|
|
NM_001201366.2:c.*200C>G
|
NP_001188295.1:n.*200C>G
|
|