ENST00000440400.3:c.733+634G>T
|
ENSP00000398393.2:n.733+634G>T
|
|
ENST00000697712.1:c.593-147G>T
|
ENSP00000513410.1:n.593-147G>T
|
|
ENST00000252699.7:c.734-147G>T
MANE Select
|
ENSP00000252699.2:n.734-147G>T
|
|
ENST00000424234.7:c.733+634G>T
|
ENSP00000411187.4:n.733+634G>T
|
|
ENST00000440400.2:c.733+634G>T
|
ENSP00000398393.2:n.733+634G>T
|
|
ENST00000252699.6:c.734-147G>T
|
ENSP00000252699.2:n.734-147G>T
|
|
ENST00000390009.7:c.163-4359G>T
|
ENSP00000439497.1:n.163-4359G>T
|
|
ENST00000424234.6:c.272+9401G>T
|
ENSP00000411187.3:n.272+9401G>T
|
|
ENST00000586538.1:c.136+634G>T
|
ENSP00000465176.1:n.136+634G>T
|
|
ENST00000588618.5:n.831-147G>T
|
|
|
ENST00000589528.1:c.285+9396G>T
|
|
|
NM_004924.4:c.734-147G>T
|
NP_004915.2:n.734-147G>T
|
|
XM_005259281.3:c.734-147G>T
|
XP_005259338.1:n.734-147G>T
|
|
XM_005259282.3:c.733+634G>T
|
XP_005259339.1:n.733+634G>T
|
|
XM_006723406.1:c.733+634G>T
|
XP_006723469.1:n.733+634G>T
|
|
NM_001322033.1:c.733+634G>T
|
NP_001308962.1:n.733+634G>T
|
|
NM_004924.5:c.734-147G>T
|
NP_004915.2:n.734-147G>T
|
|
XM_005259281.5:c.734-147G>T
|
XP_005259338.1:n.734-147G>T
|
|
XM_006723406.3:c.733+634G>T
|
XP_006723469.1:n.733+634G>T
|
|
XM_017027331.2:c.734-147G>T
|
XP_016882820.1:n.734-147G>T
|
|
XR_001753937.1:n.123-7946C>A
|
|
|
NM_004924.6:c.734-147G>T
MANE Select
|
NP_004915.2:n.734-147G>T
|
|
NM_001322033.2:c.733+634G>T
|
NP_001308962.1:n.733+634G>T
|
|