ENST00000265104.5:c.9273G=
MANE Select
|
ENSP00000265104.4:p.Val3091=
|
|
ENST00000681290.1:c.9228G=
|
ENSP00000505288.1:p.Val3076=
|
|
ENST00000265104.4:c.9273G=
|
ENSP00000265104.4:p.Val3091=
|
|
NM_001369.2:c.9273G=
|
NP_001360.1:p.Val3091=
|
|
XM_005248262.2:c.9228G=
|
XP_005248319.1:p.Val3076=
|
|
XM_005248262.3:c.9381G=
|
XP_005248319.2:p.Val3127=
|
|
XM_017009177.1:c.9381G=
|
XP_016864666.1:p.Val3127=
|
|
XM_017009178.1:c.8286G=
|
XP_016864667.1:p.Val2762=
|
|
XM_017009179.2:c.8286G=
|
XP_016864668.1:p.Val2762=
|
|
XM_017009180.1:c.9381G=
|
XP_016864669.1:p.Val3127=
|
|
XM_017009181.1:c.9381G=
|
XP_016864670.1:p.Val3127=
|
|
XM_017009182.1:c.9381G=
|
XP_016864671.1:p.Val3127=
|
|
XM_017009183.1:c.9381G=
|
XP_016864672.1:p.Val3127=
|
|
XM_017009185.1:c.4470G=
|
XP_016864674.1:p.Val1490=
|
|
XM_017009186.1:c.4023G=
|
XP_016864675.1:p.Val1341=
|
|
XM_017009188.1:c.3360G=
|
XP_016864677.1:p.Val1120=
|
|
XM_024454388.1:c.8286G=
|
XP_024310156.1:p.Val2762=
|
|
XM_024454389.1:c.7875G=
|
XP_024310157.1:p.Val2625=
|
|
NM_001369.3:c.9273G=
MANE Select
|
NP_001360.1:p.Val3091=
|
|