ENST00000452035.7:n.2149T>C
|
|
|
ENST00000483004.2:c.1541T>C
|
ENSP00000419887.2:p.Leu514Pro
|
|
ENST00000698628.1:c.1624+348T>C
|
ENSP00000513848.1:n.1624+348T>C
|
|
ENST00000698629.1:n.1934T>C
|
|
|
ENST00000698630.1:n.2473T>C
|
|
|
ENST00000698631.1:n.2474T>C
|
|
|
ENST00000698632.1:n.3268T>C
|
|
|
ENST00000698633.1:n.3158T>C
|
|
|
ENST00000698636.1:n.1979T>C
|
|
|
ENST00000425368.7:c.1757T>C
MANE Select
|
ENSP00000416561.2:p.Leu586Pro
|
|
ENST00000425368.6:c.1757T>C
|
ENSP00000416561.2:p.Leu586Pro
|
|
ENST00000456570.5:c.3263T>C
|
ENSP00000410815.1:p.Leu1088Pro
|
|
ENST00000467360.1:n.883T>C
|
|
|
ENST00000477310.1:c.2810T>C
|
ENSP00000418996.1:p.Leu937Pro
|
|
ENST00000483004.1:c.379T>C
|
|
|
NM_001710.5:c.1757T>C , LRG_136t1:c.1757T>C
|
NP_001701.2:p.Leu586Pro
|
|
NM_001710.6:c.1757T>C
MANE Select
|
NP_001701.2:p.Leu586Pro
|
|