|
NM_006846.4:c.2964+14T>G
MANE Select
|
NP_006837.2:n.2964+14T>G
|
|
ENST00000256084.8:c.2964+14T>G
MANE Select
|
ENSP00000256084.7:n.2964+14T>G
|
|
NM_001127698.1:c.3054+14T>G
|
NP_001121170.1:n.3054+14T>G
|
|
NM_001127698.2:c.3054+14T>G
|
NP_001121170.1:n.3054+14T>G
|
|
NM_006846.3:c.2964+14T>G , LRG_110t1:c.2964+14T>G
|
NP_006837.2:n.2964+14T>G
|
|
ENST00000256084.7:c.2964+14T>G
|
ENSP00000256084.7:n.2964+14T>G
|
|
ENST00000359874.7:c.3054+14T>G
|
ENSP00000352936.3:n.3054+14T>G
|
|
XM_011537550.1:c.2997+14T>G
|
XP_011535852.1:n.2997+14T>G
|
|
XM_011537551.1:c.2970+14T>G
|
XP_011535853.1:n.2970+14T>G
|
|
XM_011537551.2:c.2970+14T>G
|
XP_011535853.1:n.2970+14T>G
|