ENST00000265104.5:c.9734T>A
MANE Select
|
ENSP00000265104.4:p.Val3245Glu
|
|
ENST00000681290.1:c.9689T>A
|
ENSP00000505288.1:p.Val3230Glu
|
|
ENST00000265104.4:c.9734T>A
|
ENSP00000265104.4:p.Val3245Glu
|
|
ENST00000504001.3:n.446T>A
|
|
|
NM_001369.2:c.9734T>A
|
NP_001360.1:p.Val3245Glu
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|
XM_005248262.2:c.9689T>A
|
XP_005248319.1:p.Val3230Glu
|
|
XM_005248262.3:c.9842T>A
|
XP_005248319.2:p.Val3281Glu
|
|
XM_017009177.1:c.9842T>A
|
XP_016864666.1:p.Val3281Glu
|
|
XM_017009178.1:c.8747T>A
|
XP_016864667.1:p.Val2916Glu
|
|
XM_017009179.2:c.8747T>A
|
XP_016864668.1:p.Val2916Glu
|
|
XM_017009180.1:c.9842T>A
|
XP_016864669.1:p.Val3281Glu
|
|
XM_017009181.1:c.9842T>A
|
XP_016864670.1:p.Val3281Glu
|
|
XM_017009182.1:c.9842T>A
|
XP_016864671.1:p.Val3281Glu
|
|
XM_017009185.1:c.4931T>A
|
XP_016864674.1:p.Val1644Glu
|
|
XM_017009186.1:c.4484T>A
|
XP_016864675.1:p.Val1495Glu
|
|
XM_017009188.1:c.3821T>A
|
XP_016864677.1:p.Val1274Glu
|
|
XM_024454388.1:c.8747T>A
|
XP_024310156.1:p.Val2916Glu
|
|
XM_024454389.1:c.8336T>A
|
XP_024310157.1:p.Val2779Glu
|
|
NM_001369.3:c.9734T>A
MANE Select
|
NP_001360.1:p.Val3245Glu
|
|