ENST00000219070.9:c.732C>A
MANE Select
|
ENSP00000219070.4:p.Tyr244Ter
|
|
ENST00000219070.8:c.732C>A
|
ENSP00000219070.4:p.Tyr244Ter
|
|
ENST00000437642.6:c.582C>A
|
ENSP00000394237.2:p.Tyr194Ter
|
|
ENST00000543485.5:c.504C>A
|
ENSP00000444143.1:p.Tyr168Ter
|
|
ENST00000564864.5:c.504C>A
|
ENSP00000456096.1:p.Tyr168Ter
|
|
ENST00000570308.5:c.504C>A
|
ENSP00000461421.1:p.Tyr168Ter
|
|
NM_001127891.2:c.582C>A
|
NP_001121363.1:p.Tyr194Ter
|
|
NM_001302508.1:c.504C>A
|
NP_001289437.1:p.Tyr168Ter
|
|
NM_001302509.1:c.504C>A
|
NP_001289438.1:p.Tyr168Ter
|
|
NM_001302510.1:c.504C>A
|
NP_001289439.1:p.Tyr168Ter
|
|
NM_004530.5:c.732C>A
|
NP_004521.1:p.Tyr244Ter
|
|
NM_004530.6:c.732C>A
MANE Select
|
NP_004521.1:p.Tyr244Ter
|
|
NM_001127891.3:c.582C>A
|
NP_001121363.1:p.Tyr194Ter
|
|
NM_001302509.2:c.504C>A
|
NP_001289438.1:p.Tyr168Ter
|
|
NM_001302510.2:c.504C>A
|
NP_001289439.1:p.Tyr168Ter
|
|