ENST00000624552.4:c.14967G>C
|
ENSP00000485357.2:p.Glu4989Asp
|
|
ENST00000683500.2:c.15024G>C
MANE Select
|
ENSP00000508292.2:p.Glu5008Asp
|
|
ENST00000623487.1:n.3370G>C
|
|
|
ENST00000624552.3:c.14964G>C
|
ENSP00000485357.1:p.Glu4988Asp
|
|
NM_001291815.1:c.15024G>C
|
NP_001278744.1:p.Glu5008Asp
|
|
XM_011518465.1:c.14901G>C
|
XP_011516767.1:p.Glu4967Asp
|
|
XM_011518466.1:c.14892G>C
|
XP_011516768.1:p.Glu4964Asp
|
|
XM_011518467.1:c.14847G>C
|
XP_011516769.1:p.Glu4949Asp
|
|
NM_001291815.2:c.15024G>C
MANE Select
|
NP_001278744.1:p.Glu5008Asp
|
|
XM_011518465.2:c.14901G>C
|
XP_011516767.1:p.Glu4967Asp
|
|
XM_011518466.2:c.14892G>C
|
XP_011516768.1:p.Glu4964Asp
|
|
XM_011518467.2:c.14847G>C
|
XP_011516769.1:p.Glu4949Asp
|
|
XM_017014585.1:c.11805G>C
|
XP_016870074.1:p.Glu3935Asp
|
|
XM_017014586.1:c.7602G>C
|
XP_016870075.1:p.Glu2534Asp
|
|
XR_001746957.1:n.92+144C>G
|
|
|
XR_001746958.1:n.92+144C>G
|
|
|