ENST00000301761.7:c.*280G>T
MANE Select
|
ENSP00000301761.3:n.*280G>T
|
|
ENST00000301761.6:c.*280G>T
|
ENSP00000301761.2:n.*280G>T
|
|
ENST00000536670.5:n.396+8238G>T
|
|
|
ENST00000538594.5:c.370+8238G>T
|
ENSP00000440939.1:n.370+8238G>T
|
|
ENST00000541135.5:c.377+8231G>T
|
ENSP00000443130.1:n.377+8231G>T
|
|
ENST00000542074.1:c.*360G>T
|
ENSP00000469670.1:n.*360G>T
|
|
ENST00000543044.2:c.*160+120G>T
|
ENSP00000440219.1:n.*160+120G>T
|
|
ENST00000544025.5:n.465+8238G>T
|
|
|
ENST00000544801.5:c.370+8238G>T
|
ENSP00000442581.1:n.370+8238G>T
|
|
ENST00000544880.1:n.374+8238G>T
|
|
|
NM_017841.2:c.*280G>T , LRG_519t1:c.*280G>T
|
NP_060311.1:n.*280G>T
|
|
NM_017841.4:c.*280G>T
MANE Select
|
NP_060311.1:n.*280G>T
|
|