ENST00000302850.10:c.3234G>T
MANE Select
|
ENSP00000303830.4:p.Met1078Ile
|
|
ENST00000302850.9:c.3234G>T
|
ENSP00000303830.4:p.Met1078Ile
|
|
ENST00000341500.9:c.3198G>T
|
ENSP00000342838.4:p.Met1066Ile
|
|
ENST00000593970.1:n.80G>T
|
|
|
NM_000208.2:c.3234G>T
|
NP_000199.2:p.Met1078Ile
|
|
NM_000208.3:c.3234G>T
|
NP_000199.2:p.Met1078Ile
|
|
NM_001079817.1:c.3198G>T
|
NP_001073285.1:p.Met1066Ile
|
|
NM_001079817.2:c.3198G>T
|
NP_001073285.1:p.Met1066Ile
|
|
XM_011527988.1:c.3309G>T
|
XP_011526290.1:p.Met1103Ile
|
|
XM_011527989.1:c.3273G>T
|
XP_011526291.1:p.Met1091Ile
|
|
XM_011527988.2:c.3231G>T
|
XP_011526290.2:p.Met1077Ile
|
|
XM_011527989.3:c.3195G>T
|
XP_011526291.2:p.Met1065Ile
|
|
NM_000208.4:c.3234G>T
MANE Select
|
NP_000199.2:p.Met1078Ile
|
|
NM_001079817.3:c.3198G>T
|
NP_001073285.1:p.Met1066Ile
|
|