ENST00000452035.7:n.2307T>C
|
|
|
ENST00000483004.2:c.1604T>C
|
ENSP00000419887.2:p.Leu535Ser
|
|
ENST00000698628.1:c.1625-235T>C
|
ENSP00000513848.1:n.1625-235T>C
|
|
ENST00000698629.1:n.2092T>C
|
|
|
ENST00000698630.1:n.2536T>C
|
|
|
ENST00000698631.1:n.2537T>C
|
|
|
ENST00000698632.1:n.3426T>C
|
|
|
ENST00000698633.1:n.3316T>C
|
|
|
ENST00000425368.7:c.1820T>C
MANE Select
|
ENSP00000416561.2:p.Leu607Ser
|
|
ENST00000425368.6:c.1820T>C
|
ENSP00000416561.2:p.Leu607Ser
|
|
ENST00000456570.5:c.3326T>C
|
ENSP00000410815.1:p.Leu1109Ser
|
|
ENST00000467360.1:n.946T>C
|
|
|
ENST00000477310.1:c.2873T>C
|
ENSP00000418996.1:p.Leu958Ser
|
|
ENST00000482312.1:n.36T>C
|
|
|
ENST00000483004.1:c.442T>C
|
|
|
NM_001710.5:c.1820T>C , LRG_136t1:c.1820T>C
|
NP_001701.2:p.Leu607Ser
|
|
NM_001710.6:c.1820T>C
MANE Select
|
NP_001701.2:p.Leu607Ser
|
|