ENST00000255078.8:c.2539C>A
MANE Select
|
ENSP00000255078.4:p.Gln847Lys
|
|
ENST00000674675.1:c.684C>A
|
|
|
ENST00000674878.1:c.644C>A
|
|
|
ENST00000675118.1:c.2027C>A
|
|
|
ENST00000675389.1:n.814C>A
|
|
|
ENST00000675615.1:c.2539C>A
|
ENSP00000502413.1:p.Gln847Lys
|
|
ENST00000675648.1:n.1914C>A
|
|
|
ENST00000675916.1:c.783C>A
|
|
|
ENST00000676173.1:n.3284C>A
|
|
|
ENST00000676182.1:c.970C>A
|
|
|
ENST00000676228.1:c.*1862C>A
|
ENSP00000502375.1:n.*1862C>A
|
|
ENST00000255078.7:c.2539C>A
|
ENSP00000255078.3:p.Gln847Lys
|
|
ENST00000539064.5:n.2298C>A
|
|
|
ENST00000543739.5:n.1532C>A
|
|
|
NM_002180.2:c.2539C>A , LRG_250t1:c.2539C>A
|
NP_002171.2:p.Gln847Lys
|
|
XM_005273974.2:c.1528C>A
|
XP_005274031.1:p.Gln510Lys
|
|
XM_005273975.2:c.1411C>A
|
XP_005274032.1:p.Gln471Lys
|
|
XM_011544994.1:c.1306C>A
|
XP_011543296.1:p.Gln436Lys
|
|
XR_949903.1:n.2641C>A
|
|
|
XM_005273975.3:c.1411C>A
|
XP_005274032.1:p.Gln471Lys
|
|
XM_017017669.2:c.1528C>A
|
XP_016873158.1:p.Gln510Lys
|
|
XM_017017670.2:c.1528C>A
|
XP_016873159.1:p.Gln510Lys
|
|
XR_949903.3:n.2637C>A
|
|
|
NM_002180.3:c.2539C>A
MANE Select
|
NP_002171.2:p.Gln847Lys
|
|