ENST00000255078.8:c.858G>T
MANE Select
|
ENSP00000255078.4:p.Arg286=
|
|
ENST00000539224.2:c.987G>T
|
|
|
ENST00000674955.1:c.858G>T
|
ENSP00000502463.1:p.Arg286=
|
|
ENST00000675118.1:c.205G>T
|
|
|
ENST00000675119.1:c.147G>T
|
ENSP00000501861.1:p.Arg49=
|
|
ENST00000675305.1:c.147G>T
|
ENSP00000502365.1:p.Arg49=
|
|
ENST00000675464.1:c.147G>T
|
ENSP00000502650.1:p.Arg49=
|
|
ENST00000675615.1:c.858G>T
|
ENSP00000502413.1:p.Arg286=
|
|
ENST00000675683.1:c.245G>T
|
|
|
ENST00000676173.1:n.902G>T
|
|
|
ENST00000676228.1:c.*181G>T
|
ENSP00000502375.1:n.*181G>T
|
|
ENST00000676239.1:n.172G>T
|
|
|
ENST00000255078.7:c.858G>T
|
ENSP00000255078.3:p.Arg286=
|
|
NM_002180.2:c.858G>T , LRG_250t1:c.858G>T
|
NP_002171.2:p.Arg286=
|
|
XM_005273974.2:c.-154G>T
|
XP_005274031.1:n.-154G>T
|
|
XM_005273976.1:c.858G>T
|
XP_005274033.1:p.Arg286=
|
|
XR_247198.1:n.960G>T
|
|
|
XR_949903.1:n.960G>T
|
|
|
XM_005273976.2:c.858G>T
|
XP_005274033.1:p.Arg286=
|
|
XM_017017669.2:c.-154G>T
|
XP_016873158.1:n.-154G>T
|
|
XM_017017670.2:c.-154G>T
|
XP_016873159.1:n.-154G>T
|
|
XM_017017671.2:c.858G>T
|
XP_016873160.1:p.Arg286=
|
|
XR_949903.3:n.956G>T
|
|
|
NM_002180.3:c.858G>T
MANE Select
|
NP_002171.2:p.Arg286=
|
|