ENST00000440400.3:c.2720G>A
|
ENSP00000398393.2:p.Ter907=
|
|
ENST00000697712.1:c.2594G>A
|
ENSP00000513410.1:p.Ter865=
|
|
ENST00000252699.7:c.2735G>A
MANE Select
|
ENSP00000252699.2:p.Ter912=
|
|
ENST00000424234.7:c.2735G>A
|
ENSP00000411187.4:p.Ter912=
|
|
ENST00000440400.2:c.2720G>A
|
ENSP00000398393.2:p.Ter907=
|
|
ENST00000252699.6:c.2735G>A
|
ENSP00000252699.2:p.Ter912=
|
|
ENST00000390009.7:c.2078G>A
|
ENSP00000439497.1:p.Ter693=
|
|
ENST00000424234.6:c.1565G>A
|
ENSP00000411187.3:p.Ter522=
|
|
ENST00000440400.1:c.1028G>A
|
ENSP00000398393.1:p.Ter343=
|
|
ENST00000497637.5:n.488G>A
|
|
|
ENST00000589528.1:c.286-558G>A
|
|
|
NM_004924.4:c.2735G>A
|
NP_004915.2:p.Ter912=
|
|
XM_005259281.3:c.2720G>A
|
XP_005259338.1:p.Ter907=
|
|
XM_005259282.3:c.2720G>A
|
XP_005259339.1:p.Ter907=
|
|
XM_006723406.1:c.2735G>A
|
XP_006723469.1:p.Ter912=
|
|
NM_001322033.1:c.2720G>A
|
NP_001308962.1:p.Ter907=
|
|
NM_004924.5:c.2735G>A
|
NP_004915.2:p.Ter912=
|
|
XM_005259281.5:c.2720G>A
|
XP_005259338.1:p.Ter907=
|
|
XM_006723406.3:c.2735G>A
|
XP_006723469.1:p.Ter912=
|
|
XM_017027331.2:c.2801G>A
|
XP_016882820.1:p.Ter934=
|
|
NM_004924.6:c.2735G>A
MANE Select
|
NP_004915.2:p.Ter912=
|
|
NM_001322033.2:c.2720G>A
|
NP_001308962.1:p.Ter907=
|
|