ENST00000264028.5:c.267+110G>C
MANE Select
|
ENSP00000264028.4:n.267+110G>C
|
|
ENST00000264028.4:c.267+110G>C
|
ENSP00000264028.4:n.267+110G>C
|
|
ENST00000359415.8:c.390+110G>C
|
ENSP00000352385.4:n.390+110G>C
|
|
ENST00000392859.7:c.4-1560G>C
|
ENSP00000376599.3:n.4-1560G>C
|
|
ENST00000534182.2:c.159+218G>C
|
ENSP00000431676.1:n.159+218G>C
|
|
ENST00000614498.4:c.267+110G>C
|
ENSP00000482114.1:n.267+110G>C
|
|
NM_001142281.1:c.4-1560G>C
|
NP_001135753.1:n.4-1560G>C
|
|
NM_001655.4:c.267+110G>C
|
NP_001646.2:n.267+110G>C
|
|
XM_005271542.2:c.267+110G>C
|
XP_005271599.1:n.267+110G>C
|
|
XM_005271542.4:c.267+110G>C
|
XP_005271599.1:n.267+110G>C
|
|
NM_001655.5:c.267+110G>C
MANE Select
|
NP_001646.2:n.267+110G>C
|
|
NM_001142281.2:c.4-1560G>C
|
NP_001135753.1:n.4-1560G>C
|
|