ENST00000320700.10:c.591+14T>G
MANE Select
|
ENSP00000316938.5:n.591+14T>G
|
|
ENST00000320700.9:c.591+14T>G
|
ENSP00000316938.5:n.591+14T>G
|
|
ENST00000382437.8:c.528+14T>G
|
ENSP00000371874.4:n.528+14T>G
|
|
ENST00000564065.5:c.591+14T>G
|
ENSP00000454562.1:n.591+14T>G
|
|
ENST00000567494.5:c.591+14T>G
|
ENSP00000455358.1:n.591+14T>G
|
|
ENST00000569184.1:c.582+14T>G
|
ENSP00000455478.1:n.582+14T>G
|
|
ENST00000613572.4:c.528+14T>G
|
ENSP00000482627.1:n.528+14T>G
|
|
NM_001301680.1:c.591+14T>G
|
NP_001288609.1:n.591+14T>G
|
|
NM_001374.2:c.591+14T>G
|
NP_001365.1:n.591+14T>G
|
|
XM_011522399.1:c.864+14T>G
|
XP_011520701.1:n.864+14T>G
|
|
XM_011522399.2:c.864+14T>G
|
XP_011520701.1:n.864+14T>G
|
|
NM_001374.3:c.591+14T>G
MANE Select
|
NP_001365.1:n.591+14T>G
|
|
NM_001301680.2:c.591+14T>G
|
NP_001288609.1:n.591+14T>G
|
|