ENST00000455537.7:c.2992+119C>G
MANE Select
|
ENSP00000408979.2:n.2992+119C>G
|
|
ENST00000674619.1:c.3013+119C>G
|
ENSP00000502270.1:n.3013+119C>G
|
|
ENST00000675697.1:c.83+119C>G
|
|
|
ENST00000675737.1:n.515C>G
|
|
|
ENST00000675882.1:n.2515+119C>G
|
|
|
ENST00000675929.1:n.1550+119C>G
|
|
|
ENST00000676055.1:c.83+119C>G
|
|
|
ENST00000676437.1:c.17+119C>G
|
|
|
ENST00000676457.1:c.2887+119C>G
|
ENSP00000501588.1:n.2887+119C>G
|
|
ENST00000286452.5:c.2725+119C>G
|
ENSP00000286452.5:n.2725+119C>G
|
|
ENST00000455537.6:c.2992+119C>G
|
ENSP00000408979.2:n.2992+119C>G
|
|
ENST00000552227.1:n.275+119C>G
|
|
|
NM_004984.2:c.2992+119C>G
|
NP_004975.2:n.2992+119C>G
|
|
NM_001354705.1:c.2725+119C>G
|
NP_001341634.1:n.2725+119C>G
|
|
NM_004984.3:c.2992+119C>G
|
NP_004975.2:n.2992+119C>G
|
|
XR_002957324.1:n.3225+119C>G
|
|
|
NM_004984.4:c.2992+119C>G
MANE Select
|
NP_004975.2:n.2992+119C>G
|
|
NM_001354705.2:c.2725+119C>G
|
NP_001341634.1:n.2725+119C>G
|
|