ENST00000682565.1:c.11702T>G
|
ENSP00000507671.1:p.Leu3901Arg
|
|
ENST00000682801.1:c.11167-780T>G
|
ENSP00000507862.1:n.11167-780T>G
|
|
ENST00000682859.1:c.11702T>G
|
ENSP00000508222.1:p.Leu3901Arg
|
|
ENST00000683791.1:c.4788T>G
|
|
|
ENST00000684460.1:c.8983T>G
|
|
|
ENST00000684548.1:c.11702T>G
|
ENSP00000507421.1:p.Leu3901Arg
|
|
ENST00000684590.1:c.6149T>G
|
ENSP00000507376.1:p.Leu2050Arg
|
|
ENST00000684656.1:c.9167T>G
|
|
|
ENST00000613296.6:c.12083T>G
MANE Select
|
ENSP00000482968.1:p.Leu4028Arg
|
|
ENST00000651057.1:c.2237T>G
|
ENSP00000498504.1:p.Leu746Arg
|
|
ENST00000651434.1:c.3439T>G
|
|
|
ENST00000651750.1:c.1260+524T>G
|
|
|
ENST00000652487.1:c.3254T>G
|
|
|
ENST00000464408.3:n.258T>G
|
|
|
ENST00000484298.5:c.11957T>G
|
ENSP00000478155.1:p.Leu3986Arg
|
|
ENST00000613296.4:c.12083T>G
|
ENSP00000482968.1:p.Leu4028Arg
|
|
ENST00000620466.4:n.5886T>G
|
|
|
NM_015120.4:c.12086T>G , LRG_741t1:c.12086T>G
|
NP_055935.4:p.Leu4029Arg
|
|
NM_001378454.1:c.12083T>G
MANE Select
|
NP_001365383.1:p.Leu4028Arg
|
|