ENST00000682565.1:c.7365T>C
|
ENSP00000507671.1:p.His2455=
|
|
ENST00000682801.1:c.7365T>C
|
ENSP00000507862.1:p.His2455=
|
|
ENST00000682859.1:c.7365T>C
|
ENSP00000508222.1:p.His2455=
|
|
ENST00000683791.1:c.757T>C
|
|
|
ENST00000684460.1:c.4817T>C
|
|
|
ENST00000684548.1:c.7365T>C
|
ENSP00000507421.1:p.His2455=
|
|
ENST00000684590.1:c.1812T>C
|
ENSP00000507376.1:p.His604=
|
|
ENST00000684656.1:c.4817T>C
|
|
|
ENST00000613296.6:c.7746T>C
MANE Select
|
ENSP00000482968.1:p.His2582=
|
|
ENST00000651434.1:c.896-30070T>C
|
|
|
ENST00000423048.5:c.2577T>C
|
ENSP00000399833.1:p.His859=
|
|
ENST00000484298.5:c.7620T>C
|
ENSP00000478155.1:p.His2540=
|
|
ENST00000613296.4:c.7746T>C
|
ENSP00000482968.1:p.His2582=
|
|
ENST00000614410.4:c.7746T>C
|
ENSP00000479094.1:p.His2582=
|
|
ENST00000620466.4:n.1549T>C
|
|
|
NM_015120.4:c.7749T>C , LRG_741t1:c.7749T>C
|
NP_055935.4:p.His2583=
|
|
NM_001378454.1:c.7746T>C
MANE Select
|
NP_001365383.1:p.His2582=
|
|