ENST00000317961.9:c.4069+12G>A
MANE Select
|
ENSP00000322408.4:n.4069+12G>A
|
|
ENST00000317961.8:c.4069+12G>A
|
ENSP00000322408.4:n.4069+12G>A
|
|
ENST00000382806.6:c.3898+12G>A
|
ENSP00000372256.2:n.3898+12G>A
|
|
ENST00000440077.5:c.3946+12G>A
|
ENSP00000398543.1:n.3946+12G>A
|
|
ENST00000469599.6:n.2679G>A
|
|
|
ENST00000492117.1:n.3973G>A
|
|
|
ENST00000541639.5:c.4162+12G>A
|
ENSP00000444293.1:n.4162+12G>A
|
|
NM_001146705.1:c.4162+12G>A
|
NP_001140177.1:n.4162+12G>A
|
|
NM_001146706.1:c.3898+12G>A
|
NP_001140178.1:n.3898+12G>A
|
|
NM_004653.4:c.4069+12G>A
|
NP_004644.2:n.4069+12G>A
|
|
XM_005262560.1:c.3934+12G>A
|
XP_005262617.1:n.3934+12G>A
|
|
XM_005262561.1:c.3838+12G>A
|
XP_005262618.1:n.3838+12G>A
|
|
XM_011531468.1:c.3991+12G>A
|
XP_011529770.1:n.3991+12G>A
|
|
XR_244571.2:n.4357+12G>A
|
|
|
XR_430568.2:n.4703G>A
|
|
|
XM_005262560.3:c.3934+12G>A
|
XP_005262617.1:n.3934+12G>A
|
|
XM_005262561.3:c.3838+12G>A
|
XP_005262618.1:n.3838+12G>A
|
|
XM_011531468.3:c.3991+12G>A
|
XP_011529770.1:n.3991+12G>A
|
|
XM_024452495.1:c.2059+12G>A
|
XP_024308263.1:n.2059+12G>A
|
|
XM_024452496.1:c.1825+12G>A
|
XP_024308264.1:n.1825+12G>A
|
|
XR_001756009.2:n.4807+12G>A
|
|
|
XR_001756010.2:n.4807+12G>A
|
|
|
XR_001756011.2:n.4672+12G>A
|
|
|
XR_001756012.2:n.4820+12G>A
|
|
|
XR_001756013.2:n.4138+12G>A
|
|
|
XR_002958832.1:n.4251G>A
|
|
|
XR_002958834.1:n.4463+12G>A
|
|
|
XR_002958835.1:n.4346+12G>A
|
|
|
XR_002958836.1:n.5029+12G>A
|
|
|
XR_002958837.1:n.4836+12G>A
|
|
|
XR_244571.4:n.4356+12G>A
|
|
|
XR_430568.4:n.4702G>A
|
|
|
NM_001146706.2:c.3898+12G>A
|
NP_001140178.1:n.3898+12G>A
|
|
NM_004653.5:c.4069+12G>A
MANE Select
|
NP_004644.2:n.4069+12G>A
|
|
NM_001146705.2:c.4162+12G>A
|
NP_001140177.1:n.4162+12G>A
|
|