ENST00000317961.9:c.3262-11G>T
MANE Select
|
ENSP00000322408.4:n.3262-11G>T
|
|
ENST00000317961.8:c.3262-11G>T
|
ENSP00000322408.4:n.3262-11G>T
|
|
ENST00000382806.6:c.3091-11G>T
|
ENSP00000372256.2:n.3091-11G>T
|
|
ENST00000415360.1:c.178-11G>T
|
ENSP00000389433.1:n.178-11G>T
|
|
ENST00000440077.5:c.3139-11G>T
|
ENSP00000398543.1:n.3139-11G>T
|
|
ENST00000469599.6:n.1860-11G>T
|
|
|
ENST00000492117.1:n.3154-11G>T
|
|
|
ENST00000541639.5:c.3355-11G>T
|
ENSP00000444293.1:n.3355-11G>T
|
|
NM_001146705.1:c.3355-11G>T
|
NP_001140177.1:n.3355-11G>T
|
|
NM_001146706.1:c.3091-11G>T
|
NP_001140178.1:n.3091-11G>T
|
|
NM_004653.4:c.3262-11G>T
|
NP_004644.2:n.3262-11G>T
|
|
XM_005262560.1:c.3127-11G>T
|
XP_005262617.1:n.3127-11G>T
|
|
XM_005262561.1:c.3031-11G>T
|
XP_005262618.1:n.3031-11G>T
|
|
XM_011531468.1:c.3184-11G>T
|
XP_011529770.1:n.3184-11G>T
|
|
XR_244571.2:n.3550-11G>T
|
|
|
XR_430568.2:n.3884-11G>T
|
|
|
XM_005262560.3:c.3127-11G>T
|
XP_005262617.1:n.3127-11G>T
|
|
XM_005262561.3:c.3031-11G>T
|
XP_005262618.1:n.3031-11G>T
|
|
XM_011531468.3:c.3184-11G>T
|
XP_011529770.1:n.3184-11G>T
|
|
XM_024452495.1:c.1252-11G>T
|
XP_024308263.1:n.1252-11G>T
|
|
XM_024452496.1:c.1018-11G>T
|
XP_024308264.1:n.1018-11G>T
|
|
XR_001756009.2:n.4000-11G>T
|
|
|
XR_001756010.2:n.4000-11G>T
|
|
|
XR_001756011.2:n.3865-11G>T
|
|
|
XR_001756012.2:n.4013-11G>T
|
|
|
XR_001756013.2:n.3331-11G>T
|
|
|
XR_002958832.1:n.3432-11G>T
|
|
|
XR_002958834.1:n.3656-11G>T
|
|
|
XR_002958835.1:n.3539-11G>T
|
|
|
XR_002958836.1:n.4222-11G>T
|
|
|
XR_002958837.1:n.4029-11G>T
|
|
|
XR_244571.4:n.3549-11G>T
|
|
|
XR_430568.4:n.3883-11G>T
|
|
|
NM_001146706.2:c.3091-11G>T
|
NP_001140178.1:n.3091-11G>T
|
|
NM_004653.5:c.3262-11G>T
MANE Select
|
NP_004644.2:n.3262-11G>T
|
|
NM_001146705.2:c.3355-11G>T
|
NP_001140177.1:n.3355-11G>T
|
|