ENST00000265724.8:c.3013G>T
|
ENSP00000265724.3:p.Ala1005Ser
|
|
ENST00000622132.5:c.3013G>T
MANE Select
|
ENSP00000478255.1:p.Ala1005Ser
|
|
ENST00000265724.7:c.3013G>T
|
ENSP00000265724.3:p.Ala1005Ser
|
|
ENST00000475929.5:n.169G>T
|
|
|
ENST00000483831.1:n.571G>T
|
|
|
ENST00000488737.6:n.655G>T
|
|
|
ENST00000496821.5:n.641G>T
|
|
|
ENST00000543898.5:c.2821G>T
|
ENSP00000444095.1:p.Ala941Ser
|
|
ENST00000622132.4:c.3013G>T
|
ENSP00000478255.1:p.Ala1005Ser
|
|
NM_000927.4:c.3013G>T
|
NP_000918.2:p.Ala1005Ser
|
|
NM_001348944.1:c.3013G>T
|
NP_001335873.1:p.Ala1005Ser
|
|
NM_001348945.1:c.3223G>T
|
NP_001335874.1:p.Ala1075Ser
|
|
NM_001348946.1:c.3013G>T
|
NP_001335875.1:p.Ala1005Ser
|
|
NM_001348946.2:c.3013G>T
MANE Select
|
NP_001335875.1:p.Ala1005Ser
|
|
NM_000927.5:c.3013G>T
|
NP_000918.2:p.Ala1005Ser
|
|
NM_001348944.2:c.3013G>T
|
NP_001335873.1:p.Ala1005Ser
|
|
NM_001348945.2:c.3223G>T
|
NP_001335874.1:p.Ala1075Ser
|
|