ENST00000262367.10:c.5199T>G
MANE Select
|
ENSP00000262367.5:p.Tyr1733Ter
|
|
ENST00000262367.9:c.5199T>G
|
ENSP00000262367.5:p.Tyr1733Ter
|
|
ENST00000382070.7:c.5085T>G
|
ENSP00000371502.3:p.Tyr1695Ter
|
|
NM_001079846.1:c.5085T>G
|
NP_001073315.1:p.Tyr1695Ter
|
|
NM_004380.2:c.5199T>G
|
NP_004371.2:p.Tyr1733Ter
|
|
XM_005255124.3:c.5154T>G
|
XP_005255181.1:p.Tyr1718Ter
|
|
XM_005255125.3:c.4782T>G
|
XP_005255182.1:p.Tyr1594Ter
|
|
XM_006720848.2:c.4938T>G
|
XP_006720911.1:p.Tyr1646Ter
|
|
XM_011522380.1:c.5145T>G
|
XP_011520682.1:p.Tyr1715Ter
|
|
XM_011522381.1:c.4446T>G
|
XP_011520683.1:p.Tyr1482Ter
|
|
XM_005255124.4:c.5154T>G
|
XP_005255181.1:p.Tyr1718Ter
|
|
XM_005255125.4:c.4782T>G
|
XP_005255182.1:p.Tyr1594Ter
|
|
XM_006720848.3:c.4938T>G
|
XP_006720911.1:p.Tyr1646Ter
|
|
XM_011522381.2:c.4446T>G
|
XP_011520683.1:p.Tyr1482Ter
|
|
XM_017022944.1:c.5193T>G
|
XP_016878433.1:p.Tyr1731Ter
|
|
NM_004380.3:c.5199T>G
MANE Select
|
NP_004371.2:p.Tyr1733Ter
|
|