ENST00000394867.9:n.1358+73C>T
|
|
|
ENST00000687128.1:n.1431C>T
|
|
|
ENST00000688002.1:n.1286C>T
|
|
|
ENST00000689792.1:n.823+73C>T
|
|
|
ENST00000262948.10:c.919+73C>T
MANE Select
|
ENSP00000262948.4:n.919+73C>T
|
|
ENST00000262948.9:c.919+73C>T
|
ENSP00000262948.3:n.919+73C>T
|
|
ENST00000394867.8:c.628+73C>T
|
ENSP00000378336.1:n.628+73C>T
|
|
ENST00000595715.1:n.734+73C>T
|
|
|
ENST00000597263.5:n.169+1891C>T
|
|
|
ENST00000599021.1:c.30-1785C>T
|
|
|
ENST00000600584.5:n.1479+73C>T
|
|
|
ENST00000601786.5:n.1220+73C>T
|
|
|
NM_030662.3:c.919+73C>T , LRG_750t1:c.919+73C>T
|
NP_109587.1:n.919+73C>T
|
|
XM_006722799.2:c.705+1891C>T
|
XP_006722862.1:n.705+1891C>T
|
|
XM_011528133.1:c.349+73C>T
|
XP_011526435.1:n.349+73C>T
|
|
XM_017026989.1:c.919+73C>T
|
XP_016882478.1:n.919+73C>T
|
|
XM_017026990.1:c.705+1891C>T
|
XP_016882479.1:n.705+1891C>T
|
|
NM_030662.4:c.919+73C>T
MANE Select
|
NP_109587.1:n.919+73C>T
|
|