ENST00000394867.9:n.1592A>T
|
|
|
ENST00000688002.1:n.3304A>T
|
|
|
ENST00000688751.1:n.289A>T
|
|
|
ENST00000689792.1:n.1057A>T
|
|
|
ENST00000262948.10:c.1153A>T
MANE Select
|
ENSP00000262948.4:p.Lys385Ter
|
|
ENST00000262948.9:c.1153A>T
|
ENSP00000262948.3:p.Lys385Ter
|
|
ENST00000394867.8:c.862A>T
|
ENSP00000378336.1:p.Lys288Ter
|
|
ENST00000597263.5:n.338A>T
|
|
|
ENST00000599021.1:c.263A>T
|
|
|
ENST00000600584.5:n.2602A>T
|
|
|
ENST00000601786.5:n.1454A>T
|
|
|
NM_030662.3:c.1153A>T , LRG_750t1:c.1153A>T
|
NP_109587.1:p.Lys385Ter
|
|
XM_006722799.2:c.874A>T
|
XP_006722862.1:p.Lys292Ter
|
|
XM_011528133.1:c.583A>T
|
XP_011526435.1:p.Lys195Ter
|
|
NM_030662.4:c.1153A>T
MANE Select
|
NP_109587.1:p.Lys385Ter
|
|