ENST00000682565.1:c.11610G>T
|
ENSP00000507671.1:p.Trp3870Cys
|
|
ENST00000682801.1:c.11167-872G>T
|
ENSP00000507862.1:n.11167-872G>T
|
|
ENST00000682859.1:c.11610G>T
|
ENSP00000508222.1:p.Trp3870Cys
|
|
ENST00000683791.1:c.4696G>T
|
|
|
ENST00000684460.1:c.8891G>T
|
|
|
ENST00000684548.1:c.11610G>T
|
ENSP00000507421.1:p.Trp3870Cys
|
|
ENST00000684590.1:c.6057G>T
|
ENSP00000507376.1:p.Trp2019Cys
|
|
ENST00000684656.1:c.9075G>T
|
|
|
ENST00000613296.6:c.11991G>T
MANE Select
|
ENSP00000482968.1:p.Trp3997Cys
|
|
ENST00000651057.1:c.2145G>T
|
ENSP00000498504.1:p.Trp715Cys
|
|
ENST00000651434.1:c.3347G>T
|
|
|
ENST00000651750.1:c.1260+432G>T
|
|
|
ENST00000652487.1:c.3162G>T
|
|
|
ENST00000464408.3:n.166G>T
|
|
|
ENST00000484298.5:c.11865G>T
|
ENSP00000478155.1:p.Trp3955Cys
|
|
ENST00000613296.4:c.11991G>T
|
ENSP00000482968.1:p.Trp3997Cys
|
|
ENST00000620466.4:n.5794G>T
|
|
|
NM_015120.4:c.11994G>T , LRG_741t1:c.11994G>T
|
NP_055935.4:p.Trp3998Cys
|
|
NM_001378454.1:c.11991G>T
MANE Select
|
NP_001365383.1:p.Trp3997Cys
|
|