ENST00000255078.8:c.2530G>A
MANE Select
|
ENSP00000255078.4:p.Ala844Thr
|
|
ENST00000674675.1:c.675G>A
|
|
|
ENST00000674878.1:c.635G>A
|
|
|
ENST00000675118.1:c.2018G>A
|
|
|
ENST00000675389.1:n.805G>A
|
|
|
ENST00000675615.1:c.2530G>A
|
ENSP00000502413.1:p.Ala844Thr
|
|
ENST00000675648.1:n.1905G>A
|
|
|
ENST00000675916.1:c.774G>A
|
|
|
ENST00000676173.1:n.3275G>A
|
|
|
ENST00000676182.1:c.961G>A
|
|
|
ENST00000676228.1:c.*1853G>A
|
ENSP00000502375.1:n.*1853G>A
|
|
ENST00000255078.7:c.2530G>A
|
ENSP00000255078.3:p.Ala844Thr
|
|
ENST00000539064.5:n.2289G>A
|
|
|
ENST00000543739.5:n.1523G>A
|
|
|
NM_002180.2:c.2530G>A , LRG_250t1:c.2530G>A
|
NP_002171.2:p.Ala844Thr
|
|
XM_005273974.2:c.1519G>A
|
XP_005274031.1:p.Ala507Thr
|
|
XM_005273975.2:c.1402G>A
|
XP_005274032.1:p.Ala468Thr
|
|
XM_011544994.1:c.1297G>A
|
XP_011543296.1:p.Ala433Thr
|
|
XR_949903.1:n.2632G>A
|
|
|
XM_005273975.3:c.1402G>A
|
XP_005274032.1:p.Ala468Thr
|
|
XM_017017669.2:c.1519G>A
|
XP_016873158.1:p.Ala507Thr
|
|
XM_017017670.2:c.1519G>A
|
XP_016873159.1:p.Ala507Thr
|
|
XR_949903.3:n.2628G>A
|
|
|
NM_002180.3:c.2530G>A
MANE Select
|
NP_002171.2:p.Ala844Thr
|
|