ENST00000265724.8:c.2967G>T
|
ENSP00000265724.3:p.Gly989=
|
|
ENST00000622132.5:c.2967G>T
MANE Select
|
ENSP00000478255.1:p.Gly989=
|
|
ENST00000265724.7:c.2967G>T
|
ENSP00000265724.3:p.Gly989=
|
|
ENST00000475929.5:n.123G>T
|
|
|
ENST00000483831.1:n.525G>T
|
|
|
ENST00000488737.6:n.609G>T
|
|
|
ENST00000496821.5:n.595G>T
|
|
|
ENST00000543898.5:c.2775G>T
|
ENSP00000444095.1:p.Gly925=
|
|
ENST00000622132.4:c.2967G>T
|
ENSP00000478255.1:p.Gly989=
|
|
NM_000927.4:c.2967G>T
|
NP_000918.2:p.Gly989=
|
|
NM_001348944.1:c.2967G>T
|
NP_001335873.1:p.Gly989=
|
|
NM_001348945.1:c.3177G>T
|
NP_001335874.1:p.Gly1059=
|
|
NM_001348946.1:c.2967G>T
|
NP_001335875.1:p.Gly989=
|
|
NM_001348946.2:c.2967G>T
MANE Select
|
NP_001335875.1:p.Gly989=
|
|
NM_000927.5:c.2967G>T
|
NP_000918.2:p.Gly989=
|
|
NM_001348944.2:c.2967G>T
|
NP_001335873.1:p.Gly989=
|
|
NM_001348945.2:c.3177G>T
|
NP_001335874.1:p.Gly1059=
|
|