ENST00000394867.9:n.1486-156G>T
|
|
|
ENST00000688002.1:n.3198-156G>T
|
|
|
ENST00000688751.1:n.183-156G>T
|
|
|
ENST00000689792.1:n.951-156G>T
|
|
|
ENST00000262948.10:c.1047-156G>T
MANE Select
|
ENSP00000262948.4:n.1047-156G>T
|
|
ENST00000262948.9:c.1047-156G>T
|
ENSP00000262948.3:n.1047-156G>T
|
|
ENST00000394867.8:c.756-156G>T
|
ENSP00000378336.1:n.756-156G>T
|
|
ENST00000597263.5:n.232-156G>T
|
|
|
ENST00000599021.1:c.157-156G>T
|
|
|
ENST00000600584.5:n.2340G>T
|
|
|
ENST00000601786.5:n.1348-156G>T
|
|
|
NM_030662.3:c.1047-156G>T , LRG_750t1:c.1047-156G>T
|
NP_109587.1:n.1047-156G>T
|
|
XM_006722799.2:c.768-156G>T
|
XP_006722862.1:n.768-156G>T
|
|
XM_011528133.1:c.477-156G>T
|
XP_011526435.1:n.477-156G>T
|
|
XM_017026989.1:c.1439G>T
|
XP_016882478.1:p.Gly480Val
|
|
XM_017026990.1:c.1160G>T
|
XP_016882479.1:p.Gly387Val
|
|
NM_030662.4:c.1047-156G>T
MANE Select
|
NP_109587.1:n.1047-156G>T
|
|