ENST00000335790.8:c.239+1027G>T
MANE Select
|
ENSP00000338207.3:n.239+1027G>T
|
|
ENST00000335790.7:c.239+1027G>T
|
ENSP00000338207.3:n.239+1027G>T
|
|
ENST00000428101.6:c.236+1027G>T
|
ENSP00000404538.2:n.236+1027G>T
|
|
ENST00000524379.1:n.265+1027G>T
|
|
|
ENST00000534484.1:c.206+1027G>T
|
ENSP00000435456.1:n.206+1027G>T
|
|
NM_001270428.1:c.236+1027G>T
|
NP_001257357.1:n.236+1027G>T
|
|
NM_002315.2:c.239+1027G>T
|
NP_002306.1:n.239+1027G>T
|
|
NR_073006.1:n.755+1027G>T
|
|
|
XM_006718228.2:c.350+1027G>T
|
XP_006718291.1:n.350+1027G>T
|
|
XM_011520096.1:c.326+1027G>T
|
XP_011518398.1:n.326+1027G>T
|
|
XM_011520097.1:c.239+1027G>T
|
XP_011518399.1:n.239+1027G>T
|
|
XM_011520098.1:c.206+1027G>T
|
XP_011518400.1:n.206+1027G>T
|
|
XM_011520099.1:c.206+1027G>T
|
XP_011518401.1:n.206+1027G>T
|
|
XM_011520100.1:c.137+160G>T
|
XP_011518402.1:n.137+160G>T
|
|
XM_006718228.3:c.350+1027G>T
|
XP_006718291.1:n.350+1027G>T
|
|
XM_011520098.2:c.206+1027G>T
|
XP_011518400.1:n.206+1027G>T
|
|
XM_011520099.2:c.206+1027G>T
|
XP_011518401.1:n.206+1027G>T
|
|
NM_002315.3:c.239+1027G>T
MANE Select
|
NP_002306.1:n.239+1027G>T
|
|
NM_001270428.2:c.236+1027G>T
|
NP_001257357.1:n.236+1027G>T
|
|
NR_073006.2:n.755+1027G>T
|
|
|