ENST00000281182.9:c.1156C>G
MANE Select
|
ENSP00000281182.5:p.Gln386Glu
|
|
ENST00000281182.8:c.1156C>G
|
ENSP00000281182.4:p.Gln386Glu
|
|
ENST00000374752.6:c.775C>G
|
ENSP00000363884.4:p.Gln259Glu
|
|
ENST00000524426.5:c.*886C>G
|
ENSP00000431310.1:n.*886C>G
|
|
ENST00000524502.2:n.156C>G
|
|
|
ENST00000526026.5:c.*845C>G
|
ENSP00000431532.1:n.*845C>G
|
|
ENST00000531338.5:n.1400C>G
|
|
|
ENST00000533387.5:n.2215C>G
|
|
|
NM_014384.2:c.1156C>G , LRG_448t1:c.1156C>G
|
NP_055199.1:p.Gln386Glu
|
|
XM_005271501.2:c.1156C>G
|
XP_005271558.1:p.Gln386Glu
|
|
XM_011542750.1:c.1156C>G
|
XP_011541052.1:p.Gln386Glu
|
|
XR_947819.1:n.1220C>G
|
|
|
XR_947820.1:n.1608C>G
|
|
|
XR_947821.1:n.1365C>G
|
|
|
XR_947822.1:n.1050C>G
|
|
|
XR_947823.1:n.1206C>G
|
|
|
XM_005271505.4:c.*1421C>G
|
XP_005271562.1:n.*1421C>G
|
|
XM_011542750.3:c.1156C>G
|
XP_011541052.1:p.Gln386Glu
|
|
XM_017017542.2:c.1156C>G
|
XP_016873031.1:p.Gln386Glu
|
|
XM_017017543.2:c.1156C>G
|
XP_016873032.1:p.Gln386Glu
|
|
XM_017017544.2:c.*125C>G
|
XP_016873033.1:n.*125C>G
|
|
XM_017017545.2:c.*368C>G
|
XP_016873034.1:n.*368C>G
|
|
XM_017017546.2:c.862C>G
|
XP_016873035.1:p.Gln288Glu
|
|
XM_017017547.2:c.862C>G
|
XP_016873036.1:p.Gln288Glu
|
|
XM_017017548.2:c.*1792C>G
|
XP_016873037.1:n.*1792C>G
|
|
XM_017017549.2:c.*1566C>G
|
XP_016873038.1:n.*1566C>G
|
|
XM_024448437.1:c.*303C>G
|
XP_024304205.1:n.*303C>G
|
|
XM_024448438.1:c.775C>G
|
XP_024304206.1:p.Gln259Glu
|
|
NM_014384.3:c.1156C>G
MANE Select
|
NP_055199.1:p.Gln386Glu
|
|