|
ENST00000539696.6:c.42+231G>C
|
ENSP00000439134.1:n.42+231G>C
|
|
|
ENST00000546277.6:c.885+231G>C
|
ENSP00000438153.2:n.885+231G>C
|
|
|
ENST00000636529.2:n.524+231G>C
|
|
|
|
ENST00000697195.1:c.*649+231G>C
|
ENSP00000513181.1:n.*649+231G>C
|
|
|
ENST00000697196.1:c.*58+231G>C
|
ENSP00000513182.1:n.*58+231G>C
|
|
|
ENST00000697197.1:n.2914+231G>C
|
|
|
|
ENST00000228510.8:c.885+231G>C
MANE Select
|
ENSP00000228510.3:n.885+231G>C
|
|
|
ENST00000636529.1:c.510+231G>C
|
|
|
|
ENST00000636996.1:c.733+231G>C
|
|
|
|
ENST00000228510.7:c.885+231G>C
|
ENSP00000228510.3:n.885+231G>C
|
|
|
ENST00000392727.7:c.729+231G>C
|
ENSP00000376487.3:n.729+231G>C
|
|
|
ENST00000447878.6:c.*332+231G>C
|
ENSP00000415555.2:n.*332+231G>C
|
|
|
ENST00000537237.5:c.*558+231G>C
|
ENSP00000445382.1:n.*558+231G>C
|
|
|
ENST00000539575.4:c.885+231G>C
|
ENSP00000443551.2:n.885+231G>C
|
|
|
ENST00000539696.5:c.42+231G>C
|
ENSP00000439134.1:n.42+231G>C
|
|
|
ENST00000540353.1:n.3118+231G>C
|
|
|
|
ENST00000625889.2:c.729+231G>C
|
ENSP00000486846.1:n.729+231G>C
|
|
|
ENST00000629016.2:c.*332+231G>C
|
ENSP00000486804.1:n.*332+231G>C
|
|
|
NM_000431.3:c.885+231G>C
|
NP_000422.1:n.885+231G>C
|
|
|
NM_001114185.2:c.885+231G>C
|
NP_001107657.1:n.885+231G>C
|
|
|
NM_001301182.1:c.729+231G>C
|
NP_001288111.1:n.729+231G>C
|
|
|
XM_011538372.1:c.885+231G>C
|
XP_011536674.1:n.885+231G>C
|
|
|
XM_017019313.2:c.729+231G>C
|
XP_016874802.1:n.729+231G>C
|
|
|
XM_017019314.1:c.885+231G>C
|
XP_016874803.1:n.885+231G>C
|
|
|
XM_024448982.1:c.1116G>C
|
XP_024304750.1:p.Glu372Asp
|
|
|
NM_000431.4:c.885+231G>C
MANE Select
|
NP_000422.1:n.885+231G>C
|
|
|
NM_001114185.3:c.885+231G>C
|
NP_001107657.1:n.885+231G>C
|
|
|
NM_001301182.2:c.729+231G>C
|
NP_001288111.1:n.729+231G>C
|
|
