ENST00000406757.3:c.929C>T
|
|
|
ENST00000689310.1:c.1692C>T
|
ENSP00000510438.1:p.His564=
|
|
ENST00000692084.1:c.1027C>T
|
|
|
ENST00000370818.8:c.1740C>T
MANE Select
|
ENSP00000359854.3:p.His580=
|
|
ENST00000394299.7:c.1809C>T
|
ENSP00000377836.2:p.His603=
|
|
ENST00000669691.1:n.806C>T
|
|
|
ENST00000370818.7:c.1740C>T
|
ENSP00000359854.3:p.His580=
|
|
ENST00000394299.6:c.1809C>T
|
ENSP00000377836.2:p.His603=
|
|
ENST00000631057.2:c.1578C>T
|
ENSP00000486325.1:p.His526=
|
|
NM_001164617.1:c.1809C>T
|
NP_001158089.1:p.His603=
|
|
NM_001164618.1:c.1692C>T
|
NP_001158090.1:p.His564=
|
|
NM_001164619.1:c.1578C>T
|
NP_001158091.1:p.His526=
|
|
NM_004484.3:c.1740C>T , LRG_505t1:c.1740C>T
|
NP_004475.1:p.His580=
|
|
NM_001164617.2:c.1809C>T
|
NP_001158089.1:p.His603=
|
|
NM_001164618.2:c.1692C>T
|
NP_001158090.1:p.His564=
|
|
NM_001164619.2:c.1578C>T
|
NP_001158091.1:p.His526=
|
|
NM_004484.4:c.1740C>T
MANE Select
|
NP_004475.1:p.His580=
|
|