ENST00000455537.7:c.2984T>G
MANE Select
|
ENSP00000408979.2:p.Met995Arg
|
|
ENST00000674619.1:c.3005T>G
|
ENSP00000502270.1:p.Met1002Arg
|
|
ENST00000675697.1:c.75T>G
|
|
|
ENST00000675737.1:n.388T>G
|
|
|
ENST00000675882.1:n.2507T>G
|
|
|
ENST00000675929.1:n.1542T>G
|
|
|
ENST00000676055.1:c.75T>G
|
|
|
ENST00000676437.1:c.9T>G
|
|
|
ENST00000676457.1:c.2879T>G
|
ENSP00000501588.1:p.Met960Arg
|
|
ENST00000286452.5:c.2717T>G
|
ENSP00000286452.5:p.Met906Arg
|
|
ENST00000455537.6:c.2984T>G
|
ENSP00000408979.2:p.Met995Arg
|
|
ENST00000552227.1:n.267T>G
|
|
|
NM_004984.2:c.2984T>G
|
NP_004975.2:p.Met995Arg
|
|
NM_001354705.1:c.2717T>G
|
NP_001341634.1:p.Met906Arg
|
|
NM_004984.3:c.2984T>G
|
NP_004975.2:p.Met995Arg
|
|
XR_002957324.1:n.3217T>G
|
|
|
NM_004984.4:c.2984T>G
MANE Select
|
NP_004975.2:p.Met995Arg
|
|
NM_001354705.2:c.2717T>G
|
NP_001341634.1:p.Met906Arg
|
|