ENST00000682565.1:c.11578T>C
|
ENSP00000507671.1:p.Trp3860Arg
|
|
ENST00000682801.1:c.11167-904T>C
|
ENSP00000507862.1:n.11167-904T>C
|
|
ENST00000682859.1:c.11578T>C
|
ENSP00000508222.1:p.Trp3860Arg
|
|
ENST00000683791.1:c.4664T>C
|
|
|
ENST00000684460.1:c.8859T>C
|
|
|
ENST00000684548.1:c.11578T>C
|
ENSP00000507421.1:p.Trp3860Arg
|
|
ENST00000684590.1:c.6025T>C
|
ENSP00000507376.1:p.Trp2009Arg
|
|
ENST00000684656.1:c.9043T>C
|
|
|
ENST00000613296.6:c.11959T>C
MANE Select
|
ENSP00000482968.1:p.Trp3987Arg
|
|
ENST00000651057.1:c.2113T>C
|
ENSP00000498504.1:p.Trp705Arg
|
|
ENST00000651434.1:c.3315T>C
|
|
|
ENST00000651750.1:c.1260+400T>C
|
|
|
ENST00000652487.1:c.3130T>C
|
|
|
ENST00000464408.3:n.134T>C
|
|
|
ENST00000484298.5:c.11833T>C
|
ENSP00000478155.1:p.Trp3945Arg
|
|
ENST00000613296.4:c.11959T>C
|
ENSP00000482968.1:p.Trp3987Arg
|
|
ENST00000620466.4:n.5762T>C
|
|
|
NM_015120.4:c.11962T>C , LRG_741t1:c.11962T>C
|
NP_055935.4:p.Trp3988Arg
|
|
NM_001378454.1:c.11959T>C
MANE Select
|
NP_001365383.1:p.Trp3987Arg
|
|