ENST00000258405.9:c.1075+109G>A
|
ENSP00000258405.4:n.1075+109G>A
|
|
ENST00000409304.6:c.1072+109G>A
MANE Select
|
ENSP00000386412.1:n.1072+109G>A
|
|
ENST00000258405.8:c.1075+109G>A
|
ENSP00000258405.4:n.1075+109G>A
|
|
ENST00000409304.5:c.1072+109G>A
|
ENSP00000386412.1:n.1072+109G>A
|
|
ENST00000409840.7:c.1072+109G>A
|
ENSP00000386969.3:n.1072+109G>A
|
|
ENST00000447280.6:c.1108+109G>A
|
ENSP00000415786.2:n.1108+109G>A
|
|
ENST00000473202.1:n.2579G>A
|
|
|
ENST00000478966.1:n.505+109G>A
|
|
|
NM_001136528.1:c.1072+109G>A
|
NP_001130000.1:n.1072+109G>A
|
|
NM_001136530.1:c.1108+109G>A
|
NP_001130002.1:n.1108+109G>A
|
|
NM_006216.3:c.1075+109G>A
|
NP_006207.1:n.1075+109G>A
|
|
NR_073116.1:n.1733+109G>A
|
|
|
XM_005246641.2:c.1111+109G>A
|
XP_005246698.1:n.1111+109G>A
|
|
XM_005246642.2:c.1075+109G>A
|
XP_005246699.1:n.1075+109G>A
|
|
XM_017004330.1:c.1075+109G>A
|
XP_016859819.1:n.1075+109G>A
|
|
XM_017004332.2:c.1072+109G>A
|
XP_016859821.1:n.1072+109G>A
|
|
NM_001136528.2:c.1072+109G>A
MANE Select
|
NP_001130000.1:n.1072+109G>A
|
|
NM_006216.4:c.1075+109G>A
|
NP_006207.1:n.1075+109G>A
|
|
NR_073116.2:n.1733+109G>A
|
|
|