ENST00000624552.4:c.14965G>A
|
ENSP00000485357.2:p.Glu4989Lys
|
|
ENST00000683500.2:c.15022G>A
MANE Select
|
ENSP00000508292.2:p.Glu5008Lys
|
|
ENST00000623487.1:n.3368G>A
|
|
|
ENST00000624552.3:c.14962G>A
|
ENSP00000485357.1:p.Glu4988Lys
|
|
NM_001291815.1:c.15022G>A
|
NP_001278744.1:p.Glu5008Lys
|
|
XM_011518465.1:c.14899G>A
|
XP_011516767.1:p.Glu4967Lys
|
|
XM_011518466.1:c.14890G>A
|
XP_011516768.1:p.Glu4964Lys
|
|
XM_011518467.1:c.14845G>A
|
XP_011516769.1:p.Glu4949Lys
|
|
NM_001291815.2:c.15022G>A
MANE Select
|
NP_001278744.1:p.Glu5008Lys
|
|
XM_011518465.2:c.14899G>A
|
XP_011516767.1:p.Glu4967Lys
|
|
XM_011518466.2:c.14890G>A
|
XP_011516768.1:p.Glu4964Lys
|
|
XM_011518467.2:c.14845G>A
|
XP_011516769.1:p.Glu4949Lys
|
|
XM_017014585.1:c.11803G>A
|
XP_016870074.1:p.Glu3935Lys
|
|
XM_017014586.1:c.7600G>A
|
XP_016870075.1:p.Glu2534Lys
|
|
XR_001746957.1:n.92+146C>T
|
|
|
XR_001746958.1:n.92+146C>T
|
|
|