ENST00000265104.5:c.9139G>A
MANE Select
|
ENSP00000265104.4:p.Glu3047Lys
|
|
ENST00000681290.1:c.9094G>A
|
ENSP00000505288.1:p.Glu3032Lys
|
|
ENST00000265104.4:c.9139G>A
|
ENSP00000265104.4:p.Glu3047Lys
|
|
NM_001369.2:c.9139G>A
|
NP_001360.1:p.Glu3047Lys
|
|
XM_005248262.2:c.9094G>A
|
XP_005248319.1:p.Glu3032Lys
|
|
XM_011513990.1:c.*26G>A
|
XP_011512292.1:n.*26G>A
|
|
XR_925598.1:n.9210G>A
|
|
|
XM_005248262.3:c.9247G>A
|
XP_005248319.2:p.Glu3083Lys
|
|
XM_017009177.1:c.9247G>A
|
XP_016864666.1:p.Glu3083Lys
|
|
XM_017009178.1:c.8152G>A
|
XP_016864667.1:p.Glu2718Lys
|
|
XM_017009179.2:c.8152G>A
|
XP_016864668.1:p.Glu2718Lys
|
|
XM_017009180.1:c.9247G>A
|
XP_016864669.1:p.Glu3083Lys
|
|
XM_017009181.1:c.9247G>A
|
XP_016864670.1:p.Glu3083Lys
|
|
XM_017009182.1:c.9247G>A
|
XP_016864671.1:p.Glu3083Lys
|
|
XM_017009183.1:c.9247G>A
|
XP_016864672.1:p.Glu3083Lys
|
|
XM_017009184.1:c.*26G>A
|
XP_016864673.1:n.*26G>A
|
|
XM_017009185.1:c.4336G>A
|
XP_016864674.1:p.Glu1446Lys
|
|
XM_017009186.1:c.3889G>A
|
XP_016864675.1:p.Glu1297Lys
|
|
XM_017009188.1:c.3226G>A
|
XP_016864677.1:p.Glu1076Lys
|
|
XM_024454388.1:c.8152G>A
|
XP_024310156.1:p.Glu2718Lys
|
|
XM_024454389.1:c.7741G>A
|
XP_024310157.1:p.Glu2581Lys
|
|
XR_001742034.1:n.9133G>A
|
|
|
XR_001742035.1:n.9128G>A
|
|
|
NM_001369.3:c.9139G>A
MANE Select
|
NP_001360.1:p.Glu3047Lys
|
|