ENST00000281928.9:c.5094T>G
MANE Select
|
ENSP00000281928.3:p.Phe1698Leu
|
|
ENST00000549786.2:c.4522T>G
|
|
|
ENST00000648379.1:n.3462T>G
|
|
|
ENST00000648737.1:n.4858T>G
|
|
|
ENST00000648825.1:n.1834T>G
|
|
|
ENST00000648916.1:n.3105T>G
|
|
|
ENST00000649146.1:n.2337T>G
|
|
|
ENST00000649607.1:c.3278T>G
|
|
|
ENST00000649775.1:c.1583T>G
|
|
|
ENST00000650226.1:c.5094T>G
|
ENSP00000496981.1:p.Phe1698Leu
|
|
ENST00000281928.7:c.5094T>G
|
ENSP00000281928.3:p.Phe1698Leu
|
|
ENST00000549786.1:c.458T>G
|
|
|
ENST00000552340.1:c.126T>G
|
ENSP00000449876.1:p.Phe42Leu
|
|
NM_015335.4:c.5094T>G
|
NP_056150.1:p.Phe1698Leu
|
|
XM_011538080.1:c.5094T>G
|
XP_011536382.1:p.Phe1698Leu
|
|
XM_011538081.1:c.5091T>G
|
XP_011536383.1:p.Phe1697Leu
|
|
XM_011538082.1:c.5064T>G
|
XP_011536384.1:p.Phe1688Leu
|
|
XM_011538080.2:c.5094T>G
|
XP_011536382.1:p.Phe1698Leu
|
|
XM_011538081.2:c.5091T>G
|
XP_011536383.1:p.Phe1697Leu
|
|
XM_011538082.2:c.5064T>G
|
XP_011536384.1:p.Phe1688Leu
|
|
XM_017019090.1:c.5091T>G
|
XP_016874579.1:p.Phe1697Leu
|
|
NM_015335.5:c.5094T>G
MANE Select
|
NP_056150.1:p.Phe1698Leu
|
|