ENST00000255078.8:c.2429C>A
MANE Select
|
ENSP00000255078.4:p.Pro810His
|
|
ENST00000674675.1:c.588-14C>A
|
|
|
ENST00000674878.1:c.548-14C>A
|
|
|
ENST00000675118.1:c.1917C>A
|
|
|
ENST00000675389.1:n.704C>A
|
|
|
ENST00000675615.1:c.2429C>A
|
ENSP00000502413.1:p.Pro810His
|
|
ENST00000675648.1:n.1804C>A
|
|
|
ENST00000675916.1:c.673C>A
|
|
|
ENST00000676173.1:n.3174C>A
|
|
|
ENST00000676182.1:c.860C>A
|
|
|
ENST00000676228.1:c.*1752C>A
|
ENSP00000502375.1:n.*1752C>A
|
|
ENST00000255078.7:c.2429C>A
|
ENSP00000255078.3:p.Pro810His
|
|
ENST00000539064.5:n.2188C>A
|
|
|
ENST00000543739.5:n.1422C>A
|
|
|
NM_002180.2:c.2429C>A , LRG_250t1:c.2429C>A
|
NP_002171.2:p.Pro810His
|
|
XM_005273974.2:c.1418C>A
|
XP_005274031.1:p.Pro473His
|
|
XM_005273975.2:c.1301C>A
|
XP_005274032.1:p.Pro434His
|
|
XM_011544994.1:c.1196C>A
|
XP_011543296.1:p.Pro399His
|
|
XR_949903.1:n.2531C>A
|
|
|
XM_005273975.3:c.1301C>A
|
XP_005274032.1:p.Pro434His
|
|
XM_017017669.2:c.1418C>A
|
XP_016873158.1:p.Pro473His
|
|
XM_017017670.2:c.1418C>A
|
XP_016873159.1:p.Pro473His
|
|
XR_949903.3:n.2527C>A
|
|
|
NM_002180.3:c.2429C>A
MANE Select
|
NP_002171.2:p.Pro810His
|
|