ENST00000255078.8:c.2358C>A
MANE Select
|
ENSP00000255078.4:p.Ala786=
|
|
ENST00000674675.1:c.587+15C>A
|
|
|
ENST00000674878.1:c.547+55C>A
|
|
|
ENST00000674955.1:c.*1075C>A
|
ENSP00000502463.1:n.*1075C>A
|
|
ENST00000675118.1:c.1846C>A
|
|
|
ENST00000675389.1:n.633C>A
|
|
|
ENST00000675615.1:c.2358C>A
|
ENSP00000502413.1:p.Ala786=
|
|
ENST00000675648.1:n.1733C>A
|
|
|
ENST00000675916.1:c.602C>A
|
|
|
ENST00000676173.1:n.3103C>A
|
|
|
ENST00000676182.1:c.789C>A
|
|
|
ENST00000676228.1:c.*1681C>A
|
ENSP00000502375.1:n.*1681C>A
|
|
ENST00000255078.7:c.2358C>A
|
ENSP00000255078.3:p.Ala786=
|
|
ENST00000539064.5:n.2117C>A
|
|
|
ENST00000543739.5:n.1351C>A
|
|
|
NM_002180.2:c.2358C>A , LRG_250t1:c.2358C>A
|
NP_002171.2:p.Ala786=
|
|
XM_005273974.2:c.1347C>A
|
XP_005274031.1:p.Ala449=
|
|
XM_005273975.2:c.1230C>A
|
XP_005274032.1:p.Ala410=
|
|
XM_011544994.1:c.1125C>A
|
XP_011543296.1:p.Ala375=
|
|
XR_949903.1:n.2460C>A
|
|
|
XM_005273975.3:c.1230C>A
|
XP_005274032.1:p.Ala410=
|
|
XM_017017669.2:c.1347C>A
|
XP_016873158.1:p.Ala449=
|
|
XM_017017670.2:c.1347C>A
|
XP_016873159.1:p.Ala449=
|
|
XR_949903.3:n.2456C>A
|
|
|
NM_002180.3:c.2358C>A
MANE Select
|
NP_002171.2:p.Ala786=
|
|