ENST00000560079.7:c.3098G>T
MANE Select
|
ENSP00000452877.2:p.Arg1033Leu
|
|
ENST00000299927.4:c.3098G>T
|
ENSP00000299927.3:p.Arg1033Leu
|
|
ENST00000559607.1:c.*510G>T
|
ENSP00000453491.1:n.*510G>T
|
|
ENST00000560079.6:c.3098G>T
|
ENSP00000452877.2:p.Arg1033Leu
|
|
NM_014630.2:c.3098G>T
|
NP_055445.2:p.Arg1033Leu
|
|
XM_005254996.2:c.3098G>T
|
XP_005255053.1:p.Arg1033Leu
|
|
XM_011522246.1:c.3098G>T
|
XP_011520548.1:p.Arg1033Leu
|
|
XM_011522247.1:c.3098G>T
|
XP_011520549.1:p.Arg1033Leu
|
|
XM_011522248.1:c.3098G>T
|
XP_011520550.1:p.Arg1033Leu
|
|
XR_931951.1:n.3486G>T
|
|
|
XM_005254996.3:c.3098G>T
|
XP_005255053.1:p.Arg1033Leu
|
|
XM_011522246.2:c.3098G>T
|
XP_011520548.1:p.Arg1033Leu
|
|
XM_011522247.2:c.3098G>T
|
XP_011520549.1:p.Arg1033Leu
|
|
XM_011522248.2:c.3098G>T
|
XP_011520550.1:p.Arg1033Leu
|
|
XM_017022734.1:c.3098G>T
|
XP_016878223.1:p.Arg1033Leu
|
|
XR_931951.2:n.3491G>T
|
|
|
NM_014630.3:c.3098G>T
MANE Select
|
NP_055445.2:p.Arg1033Leu
|
|