ENST00000440400.3:c.648G>T
|
ENSP00000398393.2:p.Arg216Ser
|
|
ENST00000697712.1:c.507G>T
|
ENSP00000513410.1:p.Arg169Ser
|
|
ENST00000252699.7:c.648G>T
MANE Select
|
ENSP00000252699.2:p.Arg216Ser
|
|
ENST00000424234.7:c.648G>T
|
ENSP00000411187.4:p.Arg216Ser
|
|
ENST00000440400.2:c.648G>T
|
ENSP00000398393.2:p.Arg216Ser
|
|
ENST00000252699.6:c.648G>T
|
ENSP00000252699.2:p.Arg216Ser
|
|
ENST00000390009.7:c.163-6277G>T
|
ENSP00000439497.1:n.163-6277G>T
|
|
ENST00000424234.6:c.272+7483G>T
|
ENSP00000411187.3:n.272+7483G>T
|
|
ENST00000495553.1:n.554G>T
|
|
|
ENST00000586538.1:c.51G>T
|
ENSP00000465176.1:p.Arg17Ser
|
|
ENST00000588618.5:n.745G>T
|
|
|
ENST00000589528.1:c.285+7478G>T
|
|
|
NM_004924.4:c.648G>T
|
NP_004915.2:p.Arg216Ser
|
|
XM_005259281.3:c.648G>T
|
XP_005259338.1:p.Arg216Ser
|
|
XM_005259282.3:c.648G>T
|
XP_005259339.1:p.Arg216Ser
|
|
XM_006723406.1:c.648G>T
|
XP_006723469.1:p.Arg216Ser
|
|
NM_001322033.1:c.648G>T
|
NP_001308962.1:p.Arg216Ser
|
|
NM_004924.5:c.648G>T
|
NP_004915.2:p.Arg216Ser
|
|
XM_005259281.5:c.648G>T
|
XP_005259338.1:p.Arg216Ser
|
|
XM_006723406.3:c.648G>T
|
XP_006723469.1:p.Arg216Ser
|
|
XM_017027331.2:c.648G>T
|
XP_016882820.1:p.Arg216Ser
|
|
XR_001753937.1:n.123-6028C>A
|
|
|
NM_004924.6:c.648G>T
MANE Select
|
NP_004915.2:p.Arg216Ser
|
|
NM_001322033.2:c.648G>T
|
NP_001308962.1:p.Arg216Ser
|
|