|
NM_025074.7:c.10808+9A>G
MANE Select
|
NP_079350.5:n.10808+9A>G
|
|
ENST00000512123.4:c.10808+9A>G
MANE Select
|
ENSP00000422834.2:n.10808+9A>G
|
|
NM_025074.6:c.10808+9A>G
|
NP_079350.5:n.10808+9A>G
|
|
ENST00000512123.3:c.10808+9A>G
|
ENSP00000422834.2:n.10808+9A>G
|
|
XM_006714314.1:c.10802+9A>G
|
XP_006714377.1:n.10802+9A>G
|
|
XM_006714316.1:c.10580+9A>G
|
XP_006714379.1:n.10580+9A>G
|
|
XM_006714316.3:c.10580+9A>G
|
XP_006714379.1:n.10580+9A>G
|
|
XM_011532270.1:c.8507+9A>G
|
XP_011530572.1:n.8507+9A>G
|
|
XM_011532271.1:c.5696+9A>G
|
XP_011530573.1:n.5696+9A>G
|