ENST00000302850.10:c.4008G>T
MANE Select
|
ENSP00000303830.4:p.Gln1336His
|
|
ENST00000302850.9:c.4008G>T
|
ENSP00000303830.4:p.Gln1336His
|
|
ENST00000341500.9:c.3972G>T
|
ENSP00000342838.4:p.Gln1324His
|
|
NM_000208.2:c.4008G>T
|
NP_000199.2:p.Gln1336His
|
|
NM_000208.3:c.4008G>T
|
NP_000199.2:p.Gln1336His
|
|
NM_001079817.1:c.3972G>T
|
NP_001073285.1:p.Gln1324His
|
|
NM_001079817.2:c.3972G>T
|
NP_001073285.1:p.Gln1324His
|
|
XM_011527988.1:c.4083G>T
|
XP_011526290.1:p.Gln1361His
|
|
XM_011527989.1:c.4047G>T
|
XP_011526291.1:p.Gln1349His
|
|
XM_011527988.2:c.4005G>T
|
XP_011526290.2:p.Gln1335His
|
|
XM_011527989.3:c.3969G>T
|
XP_011526291.2:p.Gln1323His
|
|
NM_000208.4:c.4008G>T
MANE Select
|
NP_000199.2:p.Gln1336His
|
|
NM_001079817.3:c.3972G>T
|
NP_001073285.1:p.Gln1324His
|
|