ENST00000377873.8:c.956+1G>T
MANE Select
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ENSP00000367104.3:n.956+1G>T
|
|
ENST00000536626.7:c.539+1G>T
|
ENSP00000442522.1:n.539+1G>T
|
|
ENST00000377868.6:c.581+1G>T
|
ENSP00000367099.2:n.581+1G>T
|
|
ENST00000377873.7:c.956+1G>T
|
ENSP00000367104.3:n.956+1G>T
|
|
ENST00000536626.5:c.539+1G>T
|
ENSP00000442522.1:n.539+1G>T
|
|
NM_001161705.1:c.581+1G>T
|
NP_001155177.1:n.581+1G>T
|
|
NM_001195.4:c.956+1G>T
|
NP_001186.1:n.956+1G>T
|
|
NM_001278606.1:c.539+1G>T
|
NP_001265535.1:n.539+1G>T
|
|
NM_001278607.1:c.623+1G>T
|
NP_001265536.1:n.623+1G>T
|
|
NM_001278608.1:c.539+1G>T
|
NP_001265537.1:n.539+1G>T
|
|
XM_011529312.1:c.539+1G>T
|
XP_011527614.1:n.539+1G>T
|
|
XM_017028005.2:c.848+1G>T
|
XP_016883494.1:n.848+1G>T
|
|
NM_001195.5:c.956+1G>T
MANE Select
|
NP_001186.1:n.956+1G>T
|
|
NM_001161705.2:c.581+1G>T
|
NP_001155177.1:n.581+1G>T
|
|
NM_001278606.2:c.539+1G>T
|
NP_001265535.1:n.539+1G>T
|
|
NM_001278607.2:c.623+1G>T
|
NP_001265536.1:n.623+1G>T
|
|
NM_001278608.2:c.539+1G>T
|
NP_001265537.1:n.539+1G>T
|
|