ENST00000302850.10:c.3369+27G>T
MANE Select
|
ENSP00000303830.4:n.3369+27G>T
|
|
ENST00000302850.9:c.3369+27G>T
|
ENSP00000303830.4:n.3369+27G>T
|
|
ENST00000341500.9:c.3333+27G>T
|
ENSP00000342838.4:n.3333+27G>T
|
|
ENST00000593970.1:n.215+27G>T
|
|
|
ENST00000601099.1:n.280+27G>T
|
|
|
NM_000208.2:c.3369+27G>T
|
NP_000199.2:n.3369+27G>T
|
|
NM_000208.3:c.3369+27G>T
|
NP_000199.2:n.3369+27G>T
|
|
NM_001079817.1:c.3333+27G>T
|
NP_001073285.1:n.3333+27G>T
|
|
NM_001079817.2:c.3333+27G>T
|
NP_001073285.1:n.3333+27G>T
|
|
XM_011527988.1:c.3444+27G>T
|
XP_011526290.1:n.3444+27G>T
|
|
XM_011527989.1:c.3408+27G>T
|
XP_011526291.1:n.3408+27G>T
|
|
XM_011527988.2:c.3366+27G>T
|
XP_011526290.2:n.3366+27G>T
|
|
XM_011527989.3:c.3330+27G>T
|
XP_011526291.2:n.3330+27G>T
|
|
NM_000208.4:c.3369+27G>T
MANE Select
|
NP_000199.2:n.3369+27G>T
|
|
NM_001079817.3:c.3333+27G>T
|
NP_001073285.1:n.3333+27G>T
|
|