ENST00000265724.8:c.2738A>C
|
ENSP00000265724.3:p.Glu913Ala
|
|
ENST00000622132.5:c.2738A>C
MANE Select
|
ENSP00000478255.1:p.Glu913Ala
|
|
ENST00000265724.7:c.2738A>C
|
ENSP00000265724.3:p.Glu913Ala
|
|
ENST00000483831.1:n.296A>C
|
|
|
ENST00000488737.6:n.380A>C
|
|
|
ENST00000496821.5:n.366A>C
|
|
|
ENST00000543898.5:c.2546A>C
|
ENSP00000444095.1:p.Glu849Ala
|
|
ENST00000622132.4:c.2738A>C
|
ENSP00000478255.1:p.Glu913Ala
|
|
NM_000927.4:c.2738A>C
|
NP_000918.2:p.Glu913Ala
|
|
NM_001348944.1:c.2738A>C
|
NP_001335873.1:p.Glu913Ala
|
|
NM_001348945.1:c.2948A>C
|
NP_001335874.1:p.Glu983Ala
|
|
NM_001348946.1:c.2738A>C
|
NP_001335875.1:p.Glu913Ala
|
|
NM_001348946.2:c.2738A>C
MANE Select
|
NP_001335875.1:p.Glu913Ala
|
|
NM_000927.5:c.2738A>C
|
NP_000918.2:p.Glu913Ala
|
|
NM_001348944.2:c.2738A>C
|
NP_001335873.1:p.Glu913Ala
|
|
NM_001348945.2:c.2948A>C
|
NP_001335874.1:p.Glu983Ala
|
|