ENST00000394867.9:n.1445G>T
|
|
|
ENST00000688002.1:n.3157G>T
|
|
|
ENST00000688751.1:n.142G>T
|
|
|
ENST00000689792.1:n.910G>T
|
|
|
ENST00000262948.10:c.1006G>T
MANE Select
|
ENSP00000262948.4:p.Gly336Cys
|
|
ENST00000262948.9:c.1006G>T
|
ENSP00000262948.3:p.Gly336Cys
|
|
ENST00000394867.8:c.715G>T
|
ENSP00000378336.1:p.Gly239Cys
|
|
ENST00000595715.1:n.821G>T
|
|
|
ENST00000597263.5:n.191G>T
|
|
|
ENST00000599021.1:c.116G>T
|
|
|
ENST00000600584.5:n.1566G>T
|
|
|
ENST00000601786.5:n.1307G>T
|
|
|
NM_030662.3:c.1006G>T , LRG_750t1:c.1006G>T
|
NP_109587.1:p.Gly336Cys
|
|
XM_006722799.2:c.727G>T
|
XP_006722862.1:p.Gly243Cys
|
|
XM_011528133.1:c.436G>T
|
XP_011526435.1:p.Gly146Cys
|
|
XM_017026989.1:c.1006G>T
|
XP_016882478.1:p.Gly336Cys
|
|
XM_017026990.1:c.727G>T
|
XP_016882479.1:p.Gly243Cys
|
|
NM_030662.4:c.1006G>T
MANE Select
|
NP_109587.1:p.Gly336Cys
|
|