ENST00000696136.1:c.351C>A
|
ENSP00000512428.1:p.Tyr117Ter
|
|
ENST00000696137.1:c.318C>A
|
ENSP00000512429.1:p.Tyr106Ter
|
|
ENST00000696152.1:c.318C>A
|
ENSP00000512443.1:p.Tyr106Ter
|
|
ENST00000696228.1:c.351C>A
|
ENSP00000512494.1:p.Tyr117Ter
|
|
ENST00000241393.4:c.363C>A
MANE Select
|
ENSP00000241393.3:p.Tyr121Ter
|
|
ENST00000241393.3:c.363C>A
|
ENSP00000241393.3:p.Tyr121Ter
|
|
ENST00000409817.1:c.375C>A
|
ENSP00000386884.1:p.Tyr125Ter
|
|
ENST00000466288.1:n.557C>A
|
|
|
NM_001008540.1:c.375C>A
|
NP_001008540.1:p.Tyr125Ter
|
|
NM_003467.2:c.363C>A , LRG_51t1:c.363C>A
|
NP_003458.1:p.Tyr121Ter
|
|
NM_001008540.2:c.375C>A
|
NP_001008540.1:p.Tyr125Ter
|
|
NM_001348056.1:c.576C>A
|
NP_001334985.1:p.Tyr192Ter
|
|
NM_001348059.1:c.462C>A
|
NP_001334988.1:p.Tyr154Ter
|
|
NM_001348060.1:c.318C>A
|
NP_001334989.1:p.Tyr106Ter
|
|
NM_001348056.2:c.576C>A
|
NP_001334985.1:p.Tyr192Ter
|
|
NM_001348059.2:c.462C>A
|
NP_001334988.1:p.Tyr154Ter
|
|
NM_001348060.2:c.318C>A
|
NP_001334989.1:p.Tyr106Ter
|
|
NM_003467.3:c.363C>A
MANE Select
|
NP_003458.1:p.Tyr121Ter
|
|