ENST00000452035.7:n.2306T=
|
|
|
ENST00000483004.2:c.1603T=
|
ENSP00000419887.2:p.Leu535=
|
|
ENST00000698628.1:c.1625-236T=
|
ENSP00000513848.1:n.1625-236T=
|
|
ENST00000698629.1:n.2091T=
|
|
|
ENST00000698630.1:n.2535T=
|
|
|
ENST00000698631.1:n.2536T=
|
|
|
ENST00000698632.1:n.3425T=
|
|
|
ENST00000698633.1:n.3315T=
|
|
|
ENST00000425368.7:c.1819T=
MANE Select
|
ENSP00000416561.2:p.Leu607=
|
|
ENST00000425368.6:c.1819T=
|
ENSP00000416561.2:p.Leu607=
|
|
ENST00000456570.5:c.3325T=
|
ENSP00000410815.1:p.Leu1109=
|
|
ENST00000467360.1:n.945T=
|
|
|
ENST00000477310.1:c.2872T=
|
ENSP00000418996.1:p.Leu958=
|
|
ENST00000482312.1:n.35T=
|
|
|
ENST00000483004.1:c.441T=
|
|
|
NM_001710.5:c.1819T= , LRG_136t1:c.1819T=
|
NP_001701.2:p.Leu607=
|
|
NM_001710.6:c.1819T=
MANE Select
|
NP_001701.2:p.Leu607=
|
|