ENST00000265724.8:c.3282+132G>C
|
ENSP00000265724.3:n.3282+132G>C
|
|
ENST00000622132.5:c.3282+132G>C
MANE Select
|
ENSP00000478255.1:n.3282+132G>C
|
|
ENST00000265724.7:c.3282+132G>C
|
ENSP00000265724.3:n.3282+132G>C
|
|
ENST00000475929.5:n.438+132G>C
|
|
|
ENST00000488737.6:n.924+132G>C
|
|
|
ENST00000543898.5:c.3090+132G>C
|
ENSP00000444095.1:n.3090+132G>C
|
|
ENST00000622132.4:c.3282+132G>C
|
ENSP00000478255.1:n.3282+132G>C
|
|
NM_000927.4:c.3282+132G>C
|
NP_000918.2:n.3282+132G>C
|
|
NM_001348944.1:c.3282+132G>C
|
NP_001335873.1:n.3282+132G>C
|
|
NM_001348945.1:c.3492+132G>C
|
NP_001335874.1:n.3492+132G>C
|
|
NM_001348946.1:c.3282+132G>C
|
NP_001335875.1:n.3282+132G>C
|
|
NM_001348946.2:c.3282+132G>C
MANE Select
|
NP_001335875.1:n.3282+132G>C
|
|
NM_000927.5:c.3282+132G>C
|
NP_000918.2:n.3282+132G>C
|
|
NM_001348944.2:c.3282+132G>C
|
NP_001335873.1:n.3282+132G>C
|
|
NM_001348945.2:c.3492+132G>C
|
NP_001335874.1:n.3492+132G>C
|
|