ENST00000255078.8:c.1456G>T
MANE Select
|
ENSP00000255078.4:p.Val486Leu
|
|
ENST00000674955.1:c.*173G>T
|
ENSP00000502463.1:n.*173G>T
|
|
ENST00000675118.1:c.944G>T
|
|
|
ENST00000675205.1:n.183+351G>T
|
|
|
ENST00000675615.1:c.1456G>T
|
ENSP00000502413.1:p.Val486Leu
|
|
ENST00000675648.1:n.831G>T
|
|
|
ENST00000675997.1:n.113-632G>T
|
|
|
ENST00000676173.1:n.2201G>T
|
|
|
ENST00000676228.1:c.*779G>T
|
ENSP00000502375.1:n.*779G>T
|
|
ENST00000255078.7:c.1456G>T
|
ENSP00000255078.3:p.Val486Leu
|
|
ENST00000537458.5:n.573G>T
|
|
|
ENST00000539064.5:n.1215G>T
|
|
|
ENST00000541229.5:n.151G>T
|
|
|
ENST00000543739.5:n.573G>T
|
|
|
NM_002180.2:c.1456G>T , LRG_250t1:c.1456G>T
|
NP_002171.2:p.Val486Leu
|
|
XM_005273974.2:c.445G>T
|
XP_005274031.1:p.Val149Leu
|
|
XM_005273975.2:c.328G>T
|
XP_005274032.1:p.Val110Leu
|
|
XM_011544994.1:c.223G>T
|
XP_011543296.1:p.Val75Leu
|
|
XR_949903.1:n.1558G>T
|
|
|
XM_005273975.3:c.328G>T
|
XP_005274032.1:p.Val110Leu
|
|
XM_017017669.2:c.445G>T
|
XP_016873158.1:p.Val149Leu
|
|
XM_017017670.2:c.445G>T
|
XP_016873159.1:p.Val149Leu
|
|
XM_017017671.2:c.1456G>T
|
XP_016873160.1:p.Val486Leu
|
|
XR_949903.3:n.1554G>T
|
|
|
NM_002180.3:c.1456G>T
MANE Select
|
NP_002171.2:p.Val486Leu
|
|