|
ENST00000433473.8:c.625-276A>T
|
ENSP00000394863.4:n.625-276A>T
|
|
|
ENST00000439754.6:c.628-276A>T
|
ENSP00000403207.2:n.628-276A>T
|
|
|
ENST00000449045.7:c.319-276A>T
|
ENSP00000392293.2:n.319-276A>T
|
|
|
ENST00000527311.7:c.397-276A>T
|
ENSP00000436695.3:n.397-276A>T
|
|
|
ENST00000530076.6:c.-30-276A>T
|
ENSP00000434007.1:n.-30-276A>T
|
|
|
ENST00000530704.6:c.*251-276A>T
|
ENSP00000431655.1:n.*251-276A>T
|
|
|
ENST00000641083.1:c.606-276A>T
|
|
|
|
ENST00000641236.1:n.865-276A>T
|
|
|
|
ENST00000641319.1:c.628-276A>T
|
ENSP00000493128.1:n.628-276A>T
|
|
|
ENST00000641381.1:c.149-2021A>T
|
|
|
|
ENST00000641471.1:c.715-276A>T
|
ENSP00000493146.1:n.715-276A>T
|
|
|
ENST00000641691.1:c.*480-276A>T
|
ENSP00000492910.1:n.*480-276A>T
|
|
|
ENST00000641924.1:c.*57-276A>T
|
ENSP00000493063.1:n.*57-276A>T
|
|
|
ENST00000642050.2:c.628-276A>T
MANE Select
|
ENSP00000493153.1:n.628-276A>T
|
|
|
ENST00000372779.8:c.715-276A>T
|
ENSP00000361865.4:n.715-276A>T
|
|
|
ENST00000433473.7:c.628-276A>T
|
ENSP00000394863.3:n.628-276A>T
|
|
|
ENST00000439754.5:c.313-276A>T
|
ENSP00000403207.1:n.313-276A>T
|
|
|
ENST00000449045.6:c.319-276A>T
|
ENSP00000392293.2:n.319-276A>T
|
|
|
ENST00000527311.6:c.403-276A>T
|
ENSP00000436695.2:n.403-276A>T
|
|
|
ENST00000529905.5:c.628-276A>T
|
ENSP00000432053.1:n.628-276A>T
|
|
|
ENST00000530076.5:c.-30-276A>T
|
ENSP00000434007.1:n.-30-276A>T
|
|
|
ENST00000530704.5:c.*251-276A>T
|
ENSP00000431655.1:n.*251-276A>T
|
|
|
NM_000310.3:c.628-276A>T , LRG_690t1:c.628-276A>T
|
NP_000301.1:n.628-276A>T
|
|
|
NM_001142604.1:c.319-276A>T
|
NP_001136076.1:n.319-276A>T
|
|
|
XM_005271008.1:c.628-276A>T
|
XP_005271065.1:n.628-276A>T
|
|
|
NM_001363695.1:c.628-276A>T
|
NP_001350624.1:n.628-276A>T
|
|
|
NM_000310.4:c.628-276A>T
MANE Select
|
NP_000301.1:n.628-276A>T
|
|
|
NM_001142604.2:c.319-276A>T
|
NP_001136076.1:n.319-276A>T
|
|
|
NM_001363695.2:c.628-276A>T
|
NP_001350624.1:n.628-276A>T
|
|
