ENST00000230882.9:c.239G>T
MANE Select
|
ENSP00000230882.4:p.Gly80Val
|
|
ENST00000230882.8:c.239G>T
|
ENSP00000230882.4:p.Gly80Val
|
|
ENST00000357703.6:c.173G>T
|
ENSP00000350335.3:p.Gly58Val
|
|
ENST00000511135.5:c.137-5925G>T
|
ENSP00000422333.1:n.137-5925G>T
|
|
ENST00000537449.5:c.239G>T
|
ENSP00000442206.2:p.Gly80Val
|
|
ENST00000612382.4:c.239G>T
|
ENSP00000478332.1:p.Gly80Val
|
|
ENST00000612626.4:c.239G>T
|
ENSP00000479846.1:p.Gly80Val
|
|
ENST00000615111.4:c.239G>T
|
ENSP00000478291.1:p.Gly80Val
|
|
ENST00000618088.4:c.239G>T
|
ENSP00000482373.1:p.Gly80Val
|
|
ENST00000620156.4:c.260G>T
|
ENSP00000483403.1:p.Gly87Val
|
|
ENST00000622294.2:c.239G>T
|
ENSP00000483926.1:p.Gly80Val
|
|
NM_000163.4:c.239G>T
|
NP_000154.1:p.Gly80Val
|
|
NM_001242399.2:c.260G>T
|
NP_001229328.1:p.Gly87Val
|
|
NM_001242400.2:c.239G>T
|
NP_001229329.1:p.Gly80Val
|
|
NM_001242401.3:c.239G>T
|
NP_001229330.1:p.Gly80Val
|
|
NM_001242402.2:c.239G>T
|
NP_001229331.1:p.Gly80Val
|
|
NM_001242403.2:c.239G>T
|
NP_001229332.1:p.Gly80Val
|
|
NM_001242404.2:c.239G>T
|
NP_001229333.1:p.Gly80Val
|
|
NM_001242405.2:c.239G>T
|
NP_001229334.1:p.Gly80Val
|
|
NM_001242406.2:c.239G>T
|
NP_001229335.1:p.Gly80Val
|
|
NM_001242460.1:c.173G>T
|
NP_001229389.1:p.Gly58Val
|
|
NM_001242462.1:c.239G>T
|
NP_001229391.1:p.Gly80Val
|
|
XM_011514031.1:c.194G>T
|
XP_011512333.1:p.Gly65Val
|
|
NM_000163.5:c.239G>T
MANE Select
|
NP_000154.1:p.Gly80Val
|
|
NM_001242401.4:c.239G>T
|
NP_001229330.1:p.Gly80Val
|
|
NM_001242403.3:c.239G>T
|
NP_001229332.1:p.Gly80Val
|
|