ENST00000682565.1:c.11715T>C
|
ENSP00000507671.1:p.Phe3905=
|
|
ENST00000682801.1:c.11167-767T>C
|
ENSP00000507862.1:n.11167-767T>C
|
|
ENST00000682859.1:c.11715T>C
|
ENSP00000508222.1:p.Phe3905=
|
|
ENST00000683791.1:c.4801T>C
|
|
|
ENST00000684460.1:c.8996T>C
|
|
|
ENST00000684548.1:c.11715T>C
|
ENSP00000507421.1:p.Phe3905=
|
|
ENST00000684590.1:c.6162T>C
|
ENSP00000507376.1:p.Phe2054=
|
|
ENST00000684656.1:c.9180T>C
|
|
|
ENST00000613296.6:c.12096T>C
MANE Select
|
ENSP00000482968.1:p.Phe4032=
|
|
ENST00000651057.1:c.2250T>C
|
ENSP00000498504.1:p.Phe750=
|
|
ENST00000651434.1:c.3452T>C
|
|
|
ENST00000651750.1:c.1260+537T>C
|
|
|
ENST00000652487.1:c.3267T>C
|
|
|
ENST00000464408.3:n.271T>C
|
|
|
ENST00000484298.5:c.11970T>C
|
ENSP00000478155.1:p.Phe3990=
|
|
ENST00000613296.4:c.12096T>C
|
ENSP00000482968.1:p.Phe4032=
|
|
ENST00000620466.4:n.5899T>C
|
|
|
NM_015120.4:c.12099T>C , LRG_741t1:c.12099T>C
|
NP_055935.4:p.Phe4033=
|
|
NM_001378454.1:c.12096T>C
MANE Select
|
NP_001365383.1:p.Phe4032=
|
|