ENST00000682565.1:c.10122G>T
|
ENSP00000507671.1:p.Leu3374Phe
|
|
ENST00000682801.1:c.10122G>T
|
ENSP00000507862.1:p.Leu3374Phe
|
|
ENST00000682859.1:c.10122G>T
|
ENSP00000508222.1:p.Leu3374Phe
|
|
ENST00000683791.1:c.3208G>T
|
|
|
ENST00000684460.1:c.7403G>T
|
|
|
ENST00000684548.1:c.10122G>T
|
ENSP00000507421.1:p.Leu3374Phe
|
|
ENST00000684590.1:c.4569G>T
|
ENSP00000507376.1:p.Leu1523Phe
|
|
ENST00000684656.1:c.7448G>T
|
|
|
ENST00000613296.6:c.10503G>T
MANE Select
|
ENSP00000482968.1:p.Leu3501Phe
|
|
ENST00000651057.1:c.657G>T
|
ENSP00000498504.1:p.Leu219Phe
|
|
ENST00000651434.1:c.1859G>T
|
|
|
ENST00000652487.1:c.1600G>T
|
|
|
ENST00000423048.5:c.3994G>T
|
ENSP00000399833.1:n.3994G>T
|
|
ENST00000484298.5:c.10377G>T
|
ENSP00000478155.1:p.Leu3459Phe
|
|
ENST00000613296.4:c.10503G>T
|
ENSP00000482968.1:p.Leu3501Phe
|
|
ENST00000614410.4:c.10503G>T
|
ENSP00000479094.1:p.Leu3501Phe
|
|
ENST00000620466.4:n.4306G>T
|
|
|
NM_015120.4:c.10506G>T , LRG_741t1:c.10506G>T
|
NP_055935.4:p.Leu3502Phe
|
|
NM_001378454.1:c.10503G>T
MANE Select
|
NP_001365383.1:p.Leu3501Phe
|
|