ENST00000452035.7:n.263C>A
|
|
|
ENST00000483004.2:c.86C>A
|
ENSP00000419887.2:p.Ser29Tyr
|
|
ENST00000497841.6:c.86C>A
|
ENSP00000513847.1:p.Ser29Tyr
|
|
ENST00000698628.1:c.86C>A
|
ENSP00000513848.1:p.Ser29Tyr
|
|
ENST00000698629.1:n.263C>A
|
|
|
ENST00000698630.1:n.247C>A
|
|
|
ENST00000698631.1:n.242C>A
|
|
|
ENST00000698632.1:n.214C>A
|
|
|
ENST00000698633.1:n.184C>A
|
|
|
ENST00000698636.1:n.308C>A
|
|
|
ENST00000425368.7:c.86C>A
MANE Select
|
ENSP00000416561.2:p.Ser29Tyr
|
|
ENST00000425368.6:c.86C>A
|
ENSP00000416561.2:p.Ser29Tyr
|
|
ENST00000452035.6:n.86C>A
|
|
|
ENST00000456570.5:c.1592C>A
|
ENSP00000410815.1:p.Ser531Tyr
|
|
ENST00000460718.5:c.65-92C>A
|
ENSP00000417793.1:n.65-92C>A
|
|
ENST00000472581.1:n.333C>A
|
|
|
ENST00000475617.5:c.86C>A
|
ENSP00000420090.1:p.Ser29Tyr
|
|
ENST00000477310.1:c.1352-613C>A
|
ENSP00000418996.1:n.1352-613C>A
|
|
NM_001710.5:c.86C>A , LRG_136t1:c.86C>A
|
NP_001701.2:p.Ser29Tyr
|
|
NM_001710.6:c.86C>A
MANE Select
|
NP_001701.2:p.Ser29Tyr
|
|