ENST00000696136.1:c.297C>G
|
ENSP00000512428.1:p.Tyr99Ter
|
|
ENST00000696137.1:c.264C>G
|
ENSP00000512429.1:p.Tyr88Ter
|
|
ENST00000696152.1:c.264C>G
|
ENSP00000512443.1:p.Tyr88Ter
|
|
ENST00000696228.1:c.297C>G
|
ENSP00000512494.1:p.Tyr99Ter
|
|
ENST00000241393.4:c.309C>G
MANE Select
|
ENSP00000241393.3:p.Tyr103Ter
|
|
ENST00000241393.3:c.309C>G
|
ENSP00000241393.3:p.Tyr103Ter
|
|
ENST00000409817.1:c.321C>G
|
ENSP00000386884.1:p.Tyr107Ter
|
|
ENST00000466288.1:n.503C>G
|
|
|
NM_001008540.1:c.321C>G
|
NP_001008540.1:p.Tyr107Ter
|
|
NM_003467.2:c.309C>G , LRG_51t1:c.309C>G
|
NP_003458.1:p.Tyr103Ter
|
|
NM_001008540.2:c.321C>G
|
NP_001008540.1:p.Tyr107Ter
|
|
NM_001348056.1:c.522C>G
|
NP_001334985.1:p.Tyr174Ter
|
|
NM_001348059.1:c.408C>G
|
NP_001334988.1:p.Tyr136Ter
|
|
NM_001348060.1:c.264C>G
|
NP_001334989.1:p.Tyr88Ter
|
|
NM_001348056.2:c.522C>G
|
NP_001334985.1:p.Tyr174Ter
|
|
NM_001348059.2:c.408C>G
|
NP_001334988.1:p.Tyr136Ter
|
|
NM_001348060.2:c.264C>G
|
NP_001334989.1:p.Tyr88Ter
|
|
NM_003467.3:c.309C>G
MANE Select
|
NP_003458.1:p.Tyr103Ter
|
|