ENST00000302850.10:c.3014-226C>A
MANE Select
|
ENSP00000303830.4:n.3014-226C>A
|
|
ENST00000302850.9:c.3014-226C>A
|
ENSP00000303830.4:n.3014-226C>A
|
|
ENST00000341500.9:c.2978-226C>A
|
ENSP00000342838.4:n.2978-226C>A
|
|
NM_000208.2:c.3014-226C>A
|
NP_000199.2:n.3014-226C>A
|
|
NM_000208.3:c.3014-226C>A
|
NP_000199.2:n.3014-226C>A
|
|
NM_001079817.1:c.2978-226C>A
|
NP_001073285.1:n.2978-226C>A
|
|
NM_001079817.2:c.2978-226C>A
|
NP_001073285.1:n.2978-226C>A
|
|
XM_011527988.1:c.3089-226C>A
|
XP_011526290.1:n.3089-226C>A
|
|
XM_011527989.1:c.3053-226C>A
|
XP_011526291.1:n.3053-226C>A
|
|
XM_011527988.2:c.3011-226C>A
|
XP_011526290.2:n.3011-226C>A
|
|
XM_011527989.3:c.2975-226C>A
|
XP_011526291.2:n.2975-226C>A
|
|
NM_000208.4:c.3014-226C>A
MANE Select
|
NP_000199.2:n.3014-226C>A
|
|
NM_001079817.3:c.2978-226C>A
|
NP_001073285.1:n.2978-226C>A
|
|