ENST00000558767.6:c.*148G>A
|
ENSP00000507680.1:n.*148G>A
|
|
ENST00000682012.1:n.530+176G>A
|
|
|
ENST00000683593.1:n.2294G>A
|
|
|
ENST00000684363.1:c.485G>A
|
ENSP00000507314.1:n.485G>A
|
|
ENST00000684569.1:n.500+176G>A
|
|
|
ENST00000561421.6:c.455+176G>A
MANE Select
|
ENSP00000453347.2:n.455+176G>A
|
|
ENST00000646551.1:n.1942+176G>A
|
|
|
ENST00000261755.9:c.455+176G>A
|
ENSP00000261755.5:n.455+176G>A
|
|
ENST00000407106.5:c.455+176G>A
|
ENSP00000385080.1:n.455+176G>A
|
|
ENST00000537726.5:n.777G>A
|
|
|
ENST00000539156.5:c.245+176G>A
|
ENSP00000454271.1:n.245+176G>A
|
|
ENST00000558022.5:c.455+176G>A
|
ENSP00000453152.1:n.455+176G>A
|
|
ENST00000558627.1:n.383+176G>A
|
|
|
ENST00000558767.5:n.892G>A
|
|
|
ENST00000561421.5:c.455+176G>A
|
ENSP00000453347.1:n.455+176G>A
|
|
NM_000137.2:c.455+176G>A
|
NP_000128.1:n.455+176G>A
|
|
XM_024449872.1:c.455+176G>A
|
XP_024305640.1:n.455+176G>A
|
|
NM_000137.4:c.455+176G>A
MANE Select
|
NP_000128.1:n.455+176G>A
|
|
NM_001374377.1:c.455+176G>A
|
NP_001361306.1:n.455+176G>A
|
|
NM_001374380.1:c.455+176G>A
|
NP_001361309.1:n.455+176G>A
|
|