ENST00000452035.7:n.2110A>C
|
|
|
ENST00000483004.2:c.1502A>C
|
ENSP00000419887.2:p.Tyr501Ser
|
|
ENST00000698628.1:c.1624+309A>C
|
ENSP00000513848.1:n.1624+309A>C
|
|
ENST00000698629.1:n.1895A>C
|
|
|
ENST00000698630.1:n.2434A>C
|
|
|
ENST00000698631.1:n.2435A>C
|
|
|
ENST00000698632.1:n.3229A>C
|
|
|
ENST00000698633.1:n.3119A>C
|
|
|
ENST00000698636.1:n.1940A>C
|
|
|
ENST00000425368.7:c.1718A>C
MANE Select
|
ENSP00000416561.2:p.Tyr573Ser
|
|
ENST00000425368.6:c.1718A>C
|
ENSP00000416561.2:p.Tyr573Ser
|
|
ENST00000456570.5:c.3224A>C
|
ENSP00000410815.1:p.Tyr1075Ser
|
|
ENST00000467360.1:n.844A>C
|
|
|
ENST00000477310.1:c.2771A>C
|
ENSP00000418996.1:p.Tyr924Ser
|
|
ENST00000483004.1:c.340A>C
|
|
|
NM_001710.5:c.1718A>C , LRG_136t1:c.1718A>C
|
NP_001701.2:p.Tyr573Ser
|
|
NM_001710.6:c.1718A>C
MANE Select
|
NP_001701.2:p.Tyr573Ser
|
|