ENST00000682565.1:c.11648A>T
|
ENSP00000507671.1:p.His3883Leu
|
|
ENST00000682801.1:c.11167-834A>T
|
ENSP00000507862.1:n.11167-834A>T
|
|
ENST00000682859.1:c.11648A>T
|
ENSP00000508222.1:p.His3883Leu
|
|
ENST00000683791.1:c.4734A>T
|
|
|
ENST00000684460.1:c.8929A>T
|
|
|
ENST00000684548.1:c.11648A>T
|
ENSP00000507421.1:p.His3883Leu
|
|
ENST00000684590.1:c.6095A>T
|
ENSP00000507376.1:p.His2032Leu
|
|
ENST00000684656.1:c.9113A>T
|
|
|
ENST00000613296.6:c.12029A>T
MANE Select
|
ENSP00000482968.1:p.His4010Leu
|
|
ENST00000651057.1:c.2183A>T
|
ENSP00000498504.1:p.His728Leu
|
|
ENST00000651434.1:c.3385A>T
|
|
|
ENST00000651750.1:c.1260+470A>T
|
|
|
ENST00000652487.1:c.3200A>T
|
|
|
ENST00000464408.3:n.204A>T
|
|
|
ENST00000484298.5:c.11903A>T
|
ENSP00000478155.1:p.His3968Leu
|
|
ENST00000613296.4:c.12029A>T
|
ENSP00000482968.1:p.His4010Leu
|
|
ENST00000620466.4:n.5832A>T
|
|
|
NM_015120.4:c.12032A>T , LRG_741t1:c.12032A>T
|
NP_055935.4:p.His4011Leu
|
|
NM_001378454.1:c.12029A>T
MANE Select
|
NP_001365383.1:p.His4010Leu
|
|