ENST00000281928.9:c.5067A>T
MANE Select
|
ENSP00000281928.3:p.Ala1689=
|
|
ENST00000549786.2:c.4495A>T
|
|
|
ENST00000648379.1:n.3435A>T
|
|
|
ENST00000648737.1:n.4831A>T
|
|
|
ENST00000648825.1:n.1807A>T
|
|
|
ENST00000648916.1:n.3078A>T
|
|
|
ENST00000649146.1:n.2310A>T
|
|
|
ENST00000649607.1:c.3251A>T
|
|
|
ENST00000649775.1:c.1556A>T
|
|
|
ENST00000650226.1:c.5067A>T
|
ENSP00000496981.1:p.Ala1689=
|
|
ENST00000281928.7:c.5067A>T
|
ENSP00000281928.3:p.Ala1689=
|
|
ENST00000549786.1:c.431A>T
|
|
|
ENST00000552340.1:c.99A>T
|
ENSP00000449876.1:p.Ala33=
|
|
NM_015335.4:c.5067A>T
|
NP_056150.1:p.Ala1689=
|
|
XM_011538080.1:c.5067A>T
|
XP_011536382.1:p.Ala1689=
|
|
XM_011538081.1:c.5064A>T
|
XP_011536383.1:p.Ala1688=
|
|
XM_011538082.1:c.5037A>T
|
XP_011536384.1:p.Ala1679=
|
|
XM_011538080.2:c.5067A>T
|
XP_011536382.1:p.Ala1689=
|
|
XM_011538081.2:c.5064A>T
|
XP_011536383.1:p.Ala1688=
|
|
XM_011538082.2:c.5037A>T
|
XP_011536384.1:p.Ala1679=
|
|
XM_017019090.1:c.5064A>T
|
XP_016874579.1:p.Ala1688=
|
|
NM_015335.5:c.5067A>T
MANE Select
|
NP_056150.1:p.Ala1689=
|
|