ENST00000452035.7:n.2068A>C
|
|
|
ENST00000483004.2:c.1460A>C
|
ENSP00000419887.2:p.Tyr487Ser
|
|
ENST00000698628.1:c.1624+267A>C
|
ENSP00000513848.1:n.1624+267A>C
|
|
ENST00000698629.1:n.1853A>C
|
|
|
ENST00000698630.1:n.2392A>C
|
|
|
ENST00000698631.1:n.2393A>C
|
|
|
ENST00000698632.1:n.3187A>C
|
|
|
ENST00000698633.1:n.3077A>C
|
|
|
ENST00000698636.1:n.1898A>C
|
|
|
ENST00000425368.7:c.1676A>C
MANE Select
|
ENSP00000416561.2:p.Tyr559Ser
|
|
ENST00000425368.6:c.1676A>C
|
ENSP00000416561.2:p.Tyr559Ser
|
|
ENST00000456570.5:c.3182A>C
|
ENSP00000410815.1:p.Tyr1061Ser
|
|
ENST00000467360.1:n.802A>C
|
|
|
ENST00000477310.1:c.2729A>C
|
ENSP00000418996.1:p.Tyr910Ser
|
|
ENST00000483004.1:c.298A>C
|
|
|
NM_001710.5:c.1676A>C , LRG_136t1:c.1676A>C
|
NP_001701.2:p.Tyr559Ser
|
|
NM_001710.6:c.1676A>C
MANE Select
|
NP_001701.2:p.Tyr559Ser
|
|