ENST00000399744.8:c.815-10T>G
MANE Select
|
ENSP00000382648.4:n.815-10T>G
|
|
ENST00000474897.6:c.814+2704T>G
|
ENSP00000434235.2:n.814+2704T>G
|
|
ENST00000329627.11:c.815-10T>G
|
ENSP00000331106.5:n.815-10T>G
|
|
ENST00000399744.7:c.815-10T>G
|
ENSP00000382648.3:n.815-10T>G
|
|
ENST00000428061.2:c.668-10T>G
|
ENSP00000412441.2:n.668-10T>G
|
|
ENST00000474897.5:c.371+7948T>G
|
ENSP00000434235.1:n.371+7948T>G
|
|
ENST00000610387.4:c.668-10T>G
|
ENSP00000482091.1:n.668-10T>G
|
|
NM_001127649.2:c.815-10T>G
|
NP_001121121.1:n.815-10T>G
|
|
NM_001199319.1:c.668-10T>G
|
NP_001186248.1:n.668-10T>G
|
|
NM_017929.5:c.815-10T>G
|
NP_060399.1:n.815-10T>G
|
|
NM_001127649.3:c.815-10T>G
MANE Select
|
NP_001121121.1:n.815-10T>G
|
|
NM_001199319.2:c.668-10T>G
|
NP_001186248.1:n.668-10T>G
|
|
NM_017929.6:c.815-10T>G
|
NP_060399.1:n.815-10T>G
|
|