ENST00000394867.9:n.1689C>A
|
|
|
ENST00000688002.1:n.3401C>A
|
|
|
ENST00000688751.1:n.386C>A
|
|
|
ENST00000689792.1:n.1154C>A
|
|
|
ENST00000262948.10:c.*47C>A
MANE Select
|
ENSP00000262948.4:n.*47C>A
|
|
ENST00000262948.9:c.*47C>A
|
ENSP00000262948.3:n.*47C>A
|
|
ENST00000394867.8:c.*47C>A
|
ENSP00000378336.1:n.*47C>A
|
|
ENST00000597263.5:n.435C>A
|
|
|
ENST00000600584.5:n.2699C>A
|
|
|
ENST00000601786.5:n.1551C>A
|
|
|
NM_030662.3:c.*47C>A , LRG_750t1:c.*47C>A
|
NP_109587.1:n.*47C>A
|
|
XM_006722799.2:c.*47C>A
|
XP_006722862.1:n.*47C>A
|
|
XM_011528133.1:c.*47C>A
|
XP_011526435.1:n.*47C>A
|
|
NM_030662.4:c.*47C>A
MANE Select
|
NP_109587.1:n.*47C>A
|
|