ENST00000265104.5:c.9379G>C
MANE Select
|
ENSP00000265104.4:p.Glu3127Gln
|
|
ENST00000681290.1:c.9334G>C
|
ENSP00000505288.1:p.Glu3112Gln
|
|
ENST00000265104.4:c.9379G>C
|
ENSP00000265104.4:p.Glu3127Gln
|
|
ENST00000504001.3:n.91G>C
|
|
|
NM_001369.2:c.9379G>C
|
NP_001360.1:p.Glu3127Gln
|
|
XM_005248262.2:c.9334G>C
|
XP_005248319.1:p.Glu3112Gln
|
|
XM_005248262.3:c.9487G>C
|
XP_005248319.2:p.Glu3163Gln
|
|
XM_017009177.1:c.9487G>C
|
XP_016864666.1:p.Glu3163Gln
|
|
XM_017009178.1:c.8392G>C
|
XP_016864667.1:p.Glu2798Gln
|
|
XM_017009179.2:c.8392G>C
|
XP_016864668.1:p.Glu2798Gln
|
|
XM_017009180.1:c.9487G>C
|
XP_016864669.1:p.Glu3163Gln
|
|
XM_017009181.1:c.9487G>C
|
XP_016864670.1:p.Glu3163Gln
|
|
XM_017009182.1:c.9487G>C
|
XP_016864671.1:p.Glu3163Gln
|
|
XM_017009183.1:c.9487G>C
|
XP_016864672.1:p.Glu3163Gln
|
|
XM_017009185.1:c.4576G>C
|
XP_016864674.1:p.Glu1526Gln
|
|
XM_017009186.1:c.4129G>C
|
XP_016864675.1:p.Glu1377Gln
|
|
XM_017009188.1:c.3466G>C
|
XP_016864677.1:p.Glu1156Gln
|
|
XM_024454388.1:c.8392G>C
|
XP_024310156.1:p.Glu2798Gln
|
|
XM_024454389.1:c.7981G>C
|
XP_024310157.1:p.Glu2661Gln
|
|
NM_001369.3:c.9379G>C
MANE Select
|
NP_001360.1:p.Glu3127Gln
|
|