ENST00000301761.7:c.*306C>G
MANE Select
|
ENSP00000301761.3:n.*306C>G
|
|
ENST00000301761.6:c.*306C>G
|
ENSP00000301761.2:n.*306C>G
|
|
ENST00000536670.5:n.396+8264C>G
|
|
|
ENST00000538594.5:c.370+8264C>G
|
ENSP00000440939.1:n.370+8264C>G
|
|
ENST00000541135.5:c.377+8257C>G
|
ENSP00000443130.1:n.377+8257C>G
|
|
ENST00000542074.1:c.*386C>G
|
ENSP00000469670.1:n.*386C>G
|
|
ENST00000543044.2:c.*160+146C>G
|
ENSP00000440219.1:n.*160+146C>G
|
|
ENST00000544025.5:n.465+8264C>G
|
|
|
ENST00000544801.5:c.370+8264C>G
|
ENSP00000442581.1:n.370+8264C>G
|
|
ENST00000544880.1:n.374+8264C>G
|
|
|
NM_017841.2:c.*306C>G , LRG_519t1:c.*306C>G
|
NP_060311.1:n.*306C>G
|
|
NM_017841.4:c.*306C>G
MANE Select
|
NP_060311.1:n.*306C>G
|
|