ENST00000691455.1:c.*1771G>T
|
ENSP00000510265.1:n.*1771G>T
|
|
ENST00000693473.1:c.1596G>T
|
|
|
ENST00000371113.9:c.1479G>T
MANE Select
|
ENSP00000360154.4:p.Arg493=
|
|
ENST00000646010.1:c.1527G>T
|
|
|
ENST00000646914.1:c.590G>T
|
|
|
ENST00000647245.1:c.1130G>T
|
|
|
ENST00000357121.5:c.1479G>T
|
ENSP00000349635.5:p.Arg493=
|
|
ENST00000371113.8:c.1479G>T
|
ENSP00000360154.4:p.Arg493=
|
|
NM_000276.3:c.1479G>T
|
NP_000267.2:p.Arg493=
|
|
NM_001587.3:c.1479G>T
|
NP_001578.2:p.Arg493=
|
|
XM_005262422.1:c.1008G>T
|
XP_005262479.1:p.Arg336=
|
|
XM_011531342.1:c.1482G>T
|
XP_011529644.1:p.Arg494=
|
|
XM_011531343.1:c.1482G>T
|
XP_011529645.1:p.Arg494=
|
|
XM_011531344.1:c.1335G>T
|
XP_011529646.1:p.Arg445=
|
|
XM_011531345.1:c.1335G>T
|
XP_011529647.1:p.Arg445=
|
|
XM_011531346.1:c.1482G>T
|
XP_011529648.1:p.Arg494=
|
|
NM_001318784.1:c.1482G>T
|
NP_001305713.1:p.Arg494=
|
|
XM_005262422.2:c.1008G>T
|
XP_005262479.1:p.Arg336=
|
|
XM_011531344.3:c.1335G>T
|
XP_011529646.1:p.Arg445=
|
|
XM_011531345.3:c.1335G>T
|
XP_011529647.1:p.Arg445=
|
|
XM_017029554.1:c.1479G>T
|
XP_016885043.1:p.Arg493=
|
|
NM_000276.4:c.1479G>T
MANE Select
|
NP_000267.2:p.Arg493=
|
|
NM_001318784.2:c.1482G>T
|
NP_001305713.1:p.Arg494=
|
|
NM_001587.4:c.1479G>T
|
NP_001578.2:p.Arg493=
|
|