ENST00000302850.10:c.3972G>A
MANE Select
|
ENSP00000303830.4:p.Met1324Ile
|
|
ENST00000302850.9:c.3972G>A
|
ENSP00000303830.4:p.Met1324Ile
|
|
ENST00000341500.9:c.3936G>A
|
ENSP00000342838.4:p.Met1312Ile
|
|
NM_000208.2:c.3972G>A
|
NP_000199.2:p.Met1324Ile
|
|
NM_000208.3:c.3972G>A
|
NP_000199.2:p.Met1324Ile
|
|
NM_001079817.1:c.3936G>A
|
NP_001073285.1:p.Met1312Ile
|
|
NM_001079817.2:c.3936G>A
|
NP_001073285.1:p.Met1312Ile
|
|
XM_011527988.1:c.4047G>A
|
XP_011526290.1:p.Met1349Ile
|
|
XM_011527989.1:c.4011G>A
|
XP_011526291.1:p.Met1337Ile
|
|
XM_011527988.2:c.3969G>A
|
XP_011526290.2:p.Met1323Ile
|
|
XM_011527989.3:c.3933G>A
|
XP_011526291.2:p.Met1311Ile
|
|
NM_000208.4:c.3972G>A
MANE Select
|
NP_000199.2:p.Met1324Ile
|
|
NM_001079817.3:c.3936G>A
|
NP_001073285.1:p.Met1312Ile
|
|