ENST00000291281.9:c.793C>T
MANE Select
|
ENSP00000291281.3:p.His265Tyr
|
|
ENST00000291281.8:c.793C>T
|
ENSP00000291281.3:p.His265Tyr
|
|
ENST00000433867.5:c.793C>T
|
ENSP00000393978.1:p.His265Tyr
|
|
ENST00000595515.5:c.793C>T
|
ENSP00000470804.1:p.His265Tyr
|
|
ENST00000600194.5:c.322C>T
|
ENSP00000472744.1:p.His108Tyr
|
|
ENST00000601605.5:c.41-3153C>T
|
ENSP00000470442.1:n.41-3153C>T
|
|
ENST00000601806.5:c.322C>T
|
ENSP00000469106.1:p.His108Tyr
|
|
NM_001079880.1:c.793C>T
|
NP_001073349.1:p.His265Tyr
|
|
NM_001079881.1:c.793C>T
|
NP_001073350.1:p.His265Tyr
|
|
NM_001079882.1:c.322C>T
|
NP_001073351.1:p.His108Tyr
|
|
NM_016457.4:c.793C>T
|
NP_057541.2:p.His265Tyr
|
|
XM_005258716.2:c.322C>T
|
XP_005258773.2:p.His108Tyr
|
|
NM_001079880.2:c.793C>T
|
NP_001073349.1:p.His265Tyr
|
|
NM_001079881.2:c.793C>T
|
NP_001073350.1:p.His265Tyr
|
|
NM_001079882.2:c.322C>T
|
NP_001073351.1:p.His108Tyr
|
|
NM_016457.5:c.793C>T
MANE Select
|
NP_057541.2:p.His265Tyr
|
|