ENST00000394867.9:n.1538A>T
|
|
|
ENST00000688002.1:n.3250A>T
|
|
|
ENST00000688751.1:n.235A>T
|
|
|
ENST00000689792.1:n.1003A>T
|
|
|
ENST00000262948.10:c.1099A>T
MANE Select
|
ENSP00000262948.4:p.Thr367Ser
|
|
ENST00000262948.9:c.1099A>T
|
ENSP00000262948.3:p.Thr367Ser
|
|
ENST00000394867.8:c.808A>T
|
ENSP00000378336.1:p.Thr270Ser
|
|
ENST00000597263.5:n.284A>T
|
|
|
ENST00000599021.1:c.209A>T
|
|
|
ENST00000600584.5:n.2548A>T
|
|
|
ENST00000601786.5:n.1400A>T
|
|
|
NM_030662.3:c.1099A>T , LRG_750t1:c.1099A>T
|
NP_109587.1:p.Thr367Ser
|
|
XM_006722799.2:c.820A>T
|
XP_006722862.1:p.Thr274Ser
|
|
XM_011528133.1:c.529A>T
|
XP_011526435.1:p.Thr177Ser
|
|
NM_030662.4:c.1099A>T
MANE Select
|
NP_109587.1:p.Thr367Ser
|
|