ENST00000624552.4:c.14966A>C
|
ENSP00000485357.2:p.Glu4989Ala
|
|
ENST00000683500.2:c.15023A>C
MANE Select
|
ENSP00000508292.2:p.Glu5008Ala
|
|
ENST00000623487.1:n.3369A>C
|
|
|
ENST00000624552.3:c.14963A>C
|
ENSP00000485357.1:p.Glu4988Ala
|
|
NM_001291815.1:c.15023A>C
|
NP_001278744.1:p.Glu5008Ala
|
|
XM_011518465.1:c.14900A>C
|
XP_011516767.1:p.Glu4967Ala
|
|
XM_011518466.1:c.14891A>C
|
XP_011516768.1:p.Glu4964Ala
|
|
XM_011518467.1:c.14846A>C
|
XP_011516769.1:p.Glu4949Ala
|
|
NM_001291815.2:c.15023A>C
MANE Select
|
NP_001278744.1:p.Glu5008Ala
|
|
XM_011518465.2:c.14900A>C
|
XP_011516767.1:p.Glu4967Ala
|
|
XM_011518466.2:c.14891A>C
|
XP_011516768.1:p.Glu4964Ala
|
|
XM_011518467.2:c.14846A>C
|
XP_011516769.1:p.Glu4949Ala
|
|
XM_017014585.1:c.11804A>C
|
XP_016870074.1:p.Glu3935Ala
|
|
XM_017014586.1:c.7601A>C
|
XP_016870075.1:p.Glu2534Ala
|
|
XR_001746957.1:n.92+145T>G
|
|
|
XR_001746958.1:n.92+145T>G
|
|
|