ENST00000394867.9:n.1358+160T>G
|
|
|
ENST00000687128.1:n.1518T>G
|
|
|
ENST00000688002.1:n.1373T>G
|
|
|
ENST00000689792.1:n.823+160T>G
|
|
|
ENST00000262948.10:c.919+160T>G
MANE Select
|
ENSP00000262948.4:n.919+160T>G
|
|
ENST00000262948.9:c.919+160T>G
|
ENSP00000262948.3:n.919+160T>G
|
|
ENST00000394867.8:c.628+160T>G
|
ENSP00000378336.1:n.628+160T>G
|
|
ENST00000595715.1:n.734+160T>G
|
|
|
ENST00000597263.5:n.169+1978T>G
|
|
|
ENST00000599021.1:c.30-1698T>G
|
|
|
ENST00000600584.5:n.1479+160T>G
|
|
|
ENST00000601786.5:n.1220+160T>G
|
|
|
NM_030662.3:c.919+160T>G , LRG_750t1:c.919+160T>G
|
NP_109587.1:n.919+160T>G
|
|
XM_006722799.2:c.705+1978T>G
|
XP_006722862.1:n.705+1978T>G
|
|
XM_011528133.1:c.349+160T>G
|
XP_011526435.1:n.349+160T>G
|
|
XM_017026989.1:c.919+160T>G
|
XP_016882478.1:n.919+160T>G
|
|
XM_017026990.1:c.705+1978T>G
|
XP_016882479.1:n.705+1978T>G
|
|
NM_030662.4:c.919+160T>G
MANE Select
|
NP_109587.1:n.919+160T>G
|
|