ENST00000302850.10:c.2843-272G>A
MANE Select
|
ENSP00000303830.4:n.2843-272G>A
|
|
ENST00000302850.9:c.2843-272G>A
|
ENSP00000303830.4:n.2843-272G>A
|
|
ENST00000341500.9:c.2807-272G>A
|
ENSP00000342838.4:n.2807-272G>A
|
|
NM_000208.2:c.2843-272G>A
|
NP_000199.2:n.2843-272G>A
|
|
NM_000208.3:c.2843-272G>A
|
NP_000199.2:n.2843-272G>A
|
|
NM_001079817.1:c.2807-272G>A
|
NP_001073285.1:n.2807-272G>A
|
|
NM_001079817.2:c.2807-272G>A
|
NP_001073285.1:n.2807-272G>A
|
|
XM_011527988.1:c.2921-275G>A
|
XP_011526290.1:n.2921-275G>A
|
|
XM_011527989.1:c.2885-275G>A
|
XP_011526291.1:n.2885-275G>A
|
|
XM_011527988.2:c.2843-275G>A
|
XP_011526290.2:n.2843-275G>A
|
|
XM_011527989.3:c.2807-275G>A
|
XP_011526291.2:n.2807-275G>A
|
|
NM_000208.4:c.2843-272G>A
MANE Select
|
NP_000199.2:n.2843-272G>A
|
|
NM_001079817.3:c.2807-272G>A
|
NP_001073285.1:n.2807-272G>A
|
|