ENST00000255078.8:c.2195T>C
MANE Select
|
ENSP00000255078.4:p.Met732Thr
|
|
ENST00000674675.1:c.439T>C
|
|
|
ENST00000674878.1:c.439T>C
|
|
|
ENST00000674955.1:c.*912T>C
|
ENSP00000502463.1:n.*912T>C
|
|
ENST00000675118.1:c.1683T>C
|
|
|
ENST00000675389.1:n.470T>C
|
|
|
ENST00000675615.1:c.2195T>C
|
ENSP00000502413.1:p.Met732Thr
|
|
ENST00000675648.1:n.1570T>C
|
|
|
ENST00000675916.1:c.439T>C
|
|
|
ENST00000676173.1:n.2940T>C
|
|
|
ENST00000676182.1:c.626T>C
|
|
|
ENST00000676228.1:c.*1518T>C
|
ENSP00000502375.1:n.*1518T>C
|
|
ENST00000255078.7:c.2195T>C
|
ENSP00000255078.3:p.Met732Thr
|
|
ENST00000539064.5:n.1954T>C
|
|
|
ENST00000543739.5:n.1188T>C
|
|
|
NM_002180.2:c.2195T>C , LRG_250t1:c.2195T>C
|
NP_002171.2:p.Met732Thr
|
|
XM_005273974.2:c.1184T>C
|
XP_005274031.1:p.Met395Thr
|
|
XM_005273975.2:c.1067T>C
|
XP_005274032.1:p.Met356Thr
|
|
XM_011544994.1:c.962T>C
|
XP_011543296.1:p.Met321Thr
|
|
XR_949903.1:n.2297T>C
|
|
|
XM_005273975.3:c.1067T>C
|
XP_005274032.1:p.Met356Thr
|
|
XM_017017669.2:c.1184T>C
|
XP_016873158.1:p.Met395Thr
|
|
XM_017017670.2:c.1184T>C
|
XP_016873159.1:p.Met395Thr
|
|
XR_949903.3:n.2293T>C
|
|
|
NM_002180.3:c.2195T>C
MANE Select
|
NP_002171.2:p.Met732Thr
|
|