ENST00000394867.9:n.1613C>T
|
|
|
ENST00000688002.1:n.3325C>T
|
|
|
ENST00000688751.1:n.310C>T
|
|
|
ENST00000689792.1:n.1078C>T
|
|
|
ENST00000262948.10:c.1174C>T
MANE Select
|
ENSP00000262948.4:p.Pro392Ser
|
|
ENST00000262948.9:c.1174C>T
|
ENSP00000262948.3:p.Pro392Ser
|
|
ENST00000394867.8:c.883C>T
|
ENSP00000378336.1:p.Pro295Ser
|
|
ENST00000597263.5:n.359C>T
|
|
|
ENST00000599021.1:c.284C>T
|
|
|
ENST00000600584.5:n.2623C>T
|
|
|
ENST00000601786.5:n.1475C>T
|
|
|
NM_030662.3:c.1174C>T , LRG_750t1:c.1174C>T
|
NP_109587.1:p.Pro392Ser
|
|
XM_006722799.2:c.895C>T
|
XP_006722862.1:p.Pro299Ser
|
|
XM_011528133.1:c.604C>T
|
XP_011526435.1:p.Pro202Ser
|
|
NM_030662.4:c.1174C>T
MANE Select
|
NP_109587.1:p.Pro392Ser
|
|