ENST00000302850.10:c.3872A>T
MANE Select
|
ENSP00000303830.4:p.Lys1291Met
|
|
ENST00000302850.9:c.3872A>T
|
ENSP00000303830.4:p.Lys1291Met
|
|
ENST00000341500.9:c.3836A>T
|
ENSP00000342838.4:p.Lys1279Met
|
|
NM_000208.2:c.3872A>T
|
NP_000199.2:p.Lys1291Met
|
|
NM_000208.3:c.3872A>T
|
NP_000199.2:p.Lys1291Met
|
|
NM_001079817.1:c.3836A>T
|
NP_001073285.1:p.Lys1279Met
|
|
NM_001079817.2:c.3836A>T
|
NP_001073285.1:p.Lys1279Met
|
|
XM_011527988.1:c.3947A>T
|
XP_011526290.1:p.Lys1316Met
|
|
XM_011527989.1:c.3911A>T
|
XP_011526291.1:p.Lys1304Met
|
|
XM_011527988.2:c.3869A>T
|
XP_011526290.2:p.Lys1290Met
|
|
XM_011527989.3:c.3833A>T
|
XP_011526291.2:p.Lys1278Met
|
|
NM_000208.4:c.3872A>T
MANE Select
|
NP_000199.2:p.Lys1291Met
|
|
NM_001079817.3:c.3836A>T
|
NP_001073285.1:p.Lys1279Met
|
|