ENST00000262367.10:c.3914+3G>T
MANE Select
|
ENSP00000262367.5:n.3914+3G>T
|
|
ENST00000262367.9:c.3914+3G>T
|
ENSP00000262367.5:n.3914+3G>T
|
|
ENST00000382070.7:c.3800+3G>T
|
ENSP00000371502.3:n.3800+3G>T
|
|
ENST00000570939.2:c.2549+3G>T
|
ENSP00000461002.2:n.2549+3G>T
|
|
ENST00000572569.1:n.378+3G>T
|
|
|
ENST00000573517.6:c.220+3G>T
|
|
|
NM_001079846.1:c.3800+3G>T
|
NP_001073315.1:n.3800+3G>T
|
|
NM_004380.2:c.3914+3G>T
|
NP_004371.2:n.3914+3G>T
|
|
XM_005255124.3:c.3869+3G>T
|
XP_005255181.1:n.3869+3G>T
|
|
XM_005255125.3:c.3497+3G>T
|
XP_005255182.1:n.3497+3G>T
|
|
XM_006720848.2:c.3914+3G>T
|
XP_006720911.1:n.3914+3G>T
|
|
XM_011522380.1:c.3860+3G>T
|
XP_011520682.1:n.3860+3G>T
|
|
XM_011522381.1:c.3161+3G>T
|
XP_011520683.1:n.3161+3G>T
|
|
XM_005255124.4:c.3869+3G>T
|
XP_005255181.1:n.3869+3G>T
|
|
XM_005255125.4:c.3497+3G>T
|
XP_005255182.1:n.3497+3G>T
|
|
XM_006720848.3:c.3914+3G>T
|
XP_006720911.1:n.3914+3G>T
|
|
XM_011522381.2:c.3161+3G>T
|
XP_011520683.1:n.3161+3G>T
|
|
XM_017022944.1:c.3908+3G>T
|
XP_016878433.1:n.3908+3G>T
|
|
NM_004380.3:c.3914+3G>T
MANE Select
|
NP_004371.2:n.3914+3G>T
|
|