NM_138801.3:c.776+108A>G
MANE Select
|
NP_620156.1:n.776+108A>G
|
ENST00000272252.10:c.776+108A>G
MANE Select
|
ENSP00000272252.5:n.776+108A>G
|
NM_138801.2:c.776+108A>G
|
NP_620156.1:n.776+108A>G
|
ENST00000272252.9:c.776+108A>G
|
ENSP00000272252.5:n.776+108A>G
|
ENST00000410063.5:c.332+108A>G
|
ENSP00000386233.1:n.332+108A>G
|
ENST00000434934.1:c.416+108A>G
|
ENSP00000399473.1:n.416+108A>G
|
ENST00000444351.5:c.766+108A>G
|
ENSP00000409083.1:n.766+108A>G
|
XR_244925.1:n.1099+108A>G
|
|
XR_244925.2:n.1087+108A>G
|
|
XR_939976.1:n.85+3661T>C
|
|