ENST00000332351.9:c.179G>T
|
ENSP00000331327.5:p.Gly60Val
|
|
ENST00000379077.9:c.179G>T
|
ENSP00000368368.5:p.Gly60Val
|
|
ENST00000448076.9:c.179G>T
|
ENSP00000413452.5:p.Gly60Val
|
|
ENST00000452863.10:c.179G>T
MANE Select
|
ENSP00000415516.5:p.Gly60Val
|
|
ENST00000639563.3:c.179G>T
|
ENSP00000492269.3:p.Gly60Val
|
|
ENST00000332351.7:c.164G>T
|
ENSP00000331327.3:p.Gly55Val
|
|
ENST00000379077.7:c.164G>T
|
ENSP00000368368.3:p.Gly55Val
|
|
ENST00000448076.7:c.164G>T
|
ENSP00000413452.3:p.Gly55Val
|
|
ENST00000452863.7:c.164G>T
|
ENSP00000415516.3:p.Gly55Val
|
|
NM_000378.4:c.164G>T
|
NP_000369.3:p.Gly55Val
|
|
NM_024424.3:c.164G>T
|
NP_077742.2:p.Gly55Val
|
|
NM_024426.4:c.164G>T
|
NP_077744.3:p.Gly55Val
|
|
NM_000378.5:c.179G>T
|
NP_000369.4:p.Gly60Val
|
|
NM_024424.4:c.179G>T
|
NP_077742.3:p.Gly60Val
|
|
NM_024426.5:c.179G>T
|
NP_077744.4:p.Gly60Val
|
|
NR_160306.1:n.358G>T
|
|
|
NM_000378.6:c.179G>T
|
NP_000369.4:p.Gly60Val
|
|
NM_024424.5:c.179G>T
|
NP_077742.3:p.Gly60Val
|
|
NM_024426.6:c.179G>T
MANE Select
|
NP_077744.4:p.Gly60Val
|
|