ENST00000682565.1:c.11620C>T
|
ENSP00000507671.1:p.Leu3874=
|
|
ENST00000682801.1:c.11167-862C>T
|
ENSP00000507862.1:n.11167-862C>T
|
|
ENST00000682859.1:c.11620C>T
|
ENSP00000508222.1:p.Leu3874=
|
|
ENST00000683791.1:c.4706C>T
|
|
|
ENST00000684460.1:c.8901C>T
|
|
|
ENST00000684548.1:c.11620C>T
|
ENSP00000507421.1:p.Leu3874=
|
|
ENST00000684590.1:c.6067C>T
|
ENSP00000507376.1:p.Leu2023=
|
|
ENST00000684656.1:c.9085C>T
|
|
|
ENST00000613296.6:c.12001C>T
MANE Select
|
ENSP00000482968.1:p.Leu4001=
|
|
ENST00000651057.1:c.2155C>T
|
ENSP00000498504.1:p.Leu719=
|
|
ENST00000651434.1:c.3357C>T
|
|
|
ENST00000651750.1:c.1260+442C>T
|
|
|
ENST00000652487.1:c.3172C>T
|
|
|
ENST00000464408.3:n.176C>T
|
|
|
ENST00000484298.5:c.11875C>T
|
ENSP00000478155.1:p.Leu3959=
|
|
ENST00000613296.4:c.12001C>T
|
ENSP00000482968.1:p.Leu4001=
|
|
ENST00000620466.4:n.5804C>T
|
|
|
NM_015120.4:c.12004C>T , LRG_741t1:c.12004C>T
|
NP_055935.4:p.Leu4002=
|
|
NM_001378454.1:c.12001C>T
MANE Select
|
NP_001365383.1:p.Leu4001=
|
|