ENST00000440400.3:c.733+859C>T
|
ENSP00000398393.2:n.733+859C>T
|
|
ENST00000697712.1:c.671C>T
|
ENSP00000513410.1:p.Ala224Val
|
|
ENST00000252699.7:c.812C>T
MANE Select
|
ENSP00000252699.2:p.Ala271Val
|
|
ENST00000424234.7:c.733+859C>T
|
ENSP00000411187.4:n.733+859C>T
|
|
ENST00000440400.2:c.733+859C>T
|
ENSP00000398393.2:n.733+859C>T
|
|
ENST00000252699.6:c.812C>T
|
ENSP00000252699.2:p.Ala271Val
|
|
ENST00000390009.7:c.163-4134C>T
|
ENSP00000439497.1:n.163-4134C>T
|
|
ENST00000424234.6:c.272+9626C>T
|
ENSP00000411187.3:n.272+9626C>T
|
|
ENST00000586538.1:c.136+859C>T
|
ENSP00000465176.1:n.136+859C>T
|
|
ENST00000588618.5:n.909C>T
|
|
|
ENST00000589528.1:c.285+9621C>T
|
|
|
NM_004924.4:c.812C>T
|
NP_004915.2:p.Ala271Val
|
|
XM_005259281.3:c.812C>T
|
XP_005259338.1:p.Ala271Val
|
|
XM_005259282.3:c.733+859C>T
|
XP_005259339.1:n.733+859C>T
|
|
XM_006723406.1:c.733+859C>T
|
XP_006723469.1:n.733+859C>T
|
|
NM_001322033.1:c.733+859C>T
|
NP_001308962.1:n.733+859C>T
|
|
NM_004924.5:c.812C>T
|
NP_004915.2:p.Ala271Val
|
|
XM_005259281.5:c.812C>T
|
XP_005259338.1:p.Ala271Val
|
|
XM_006723406.3:c.733+859C>T
|
XP_006723469.1:n.733+859C>T
|
|
XM_017027331.2:c.812C>T
|
XP_016882820.1:p.Ala271Val
|
|
XR_001753937.1:n.123-8171G>A
|
|
|
NM_004924.6:c.812C>T
MANE Select
|
NP_004915.2:p.Ala271Val
|
|
NM_001322033.2:c.733+859C>T
|
NP_001308962.1:n.733+859C>T
|
|