ENST00000394867.9:n.1540C>T
|
|
|
ENST00000688002.1:n.3252C>T
|
|
|
ENST00000688751.1:n.237C>T
|
|
|
ENST00000689792.1:n.1005C>T
|
|
|
ENST00000262948.10:c.1101C>T
MANE Select
|
ENSP00000262948.4:p.Thr367=
|
|
ENST00000262948.9:c.1101C>T
|
ENSP00000262948.3:p.Thr367=
|
|
ENST00000394867.8:c.810C>T
|
ENSP00000378336.1:p.Thr270=
|
|
ENST00000597263.5:n.286C>T
|
|
|
ENST00000599021.1:c.211C>T
|
|
|
ENST00000600584.5:n.2550C>T
|
|
|
ENST00000601786.5:n.1402C>T
|
|
|
NM_030662.3:c.1101C>T , LRG_750t1:c.1101C>T
|
NP_109587.1:p.Thr367=
|
|
XM_006722799.2:c.822C>T
|
XP_006722862.1:p.Thr274=
|
|
XM_011528133.1:c.531C>T
|
XP_011526435.1:p.Thr177=
|
|
NM_030662.4:c.1101C>T
MANE Select
|
NP_109587.1:p.Thr367=
|
|