ENST00000682565.1:c.11660G>T
|
ENSP00000507671.1:p.Arg3887Leu
|
|
ENST00000682801.1:c.11167-822G>T
|
ENSP00000507862.1:n.11167-822G>T
|
|
ENST00000682859.1:c.11660G>T
|
ENSP00000508222.1:p.Arg3887Leu
|
|
ENST00000683791.1:c.4746G>T
|
|
|
ENST00000684460.1:c.8941G>T
|
|
|
ENST00000684548.1:c.11660G>T
|
ENSP00000507421.1:p.Arg3887Leu
|
|
ENST00000684590.1:c.6107G>T
|
ENSP00000507376.1:p.Arg2036Leu
|
|
ENST00000684656.1:c.9125G>T
|
|
|
ENST00000613296.6:c.12041G>T
MANE Select
|
ENSP00000482968.1:p.Arg4014Leu
|
|
ENST00000651057.1:c.2195G>T
|
ENSP00000498504.1:p.Arg732Leu
|
|
ENST00000651434.1:c.3397G>T
|
|
|
ENST00000651750.1:c.1260+482G>T
|
|
|
ENST00000652487.1:c.3212G>T
|
|
|
ENST00000464408.3:n.216G>T
|
|
|
ENST00000484298.5:c.11915G>T
|
ENSP00000478155.1:p.Arg3972Leu
|
|
ENST00000613296.4:c.12041G>T
|
ENSP00000482968.1:p.Arg4014Leu
|
|
ENST00000620466.4:n.5844G>T
|
|
|
NM_015120.4:c.12044G>T , LRG_741t1:c.12044G>T
|
NP_055935.4:p.Arg4015Leu
|
|
NM_001378454.1:c.12041G>T
MANE Select
|
NP_001365383.1:p.Arg4014Leu
|
|