ENST00000265104.5:c.9106G=
MANE Select
|
ENSP00000265104.4:p.Val3036=
|
|
ENST00000681290.1:c.9061G=
|
ENSP00000505288.1:p.Val3021=
|
|
ENST00000265104.4:c.9106G=
|
ENSP00000265104.4:p.Val3036=
|
|
NM_001369.2:c.9106G=
|
NP_001360.1:p.Val3036=
|
|
XM_005248262.2:c.9061G=
|
XP_005248319.1:p.Val3021=
|
|
XM_011513990.1:c.9101G=
|
XP_011512292.1:p.Gly3034=
|
|
XR_925598.1:n.9177G=
|
|
|
XM_005248262.3:c.9214G=
|
XP_005248319.2:p.Val3072=
|
|
XM_017009177.1:c.9214G=
|
XP_016864666.1:p.Val3072=
|
|
XM_017009178.1:c.8119G=
|
XP_016864667.1:p.Val2707=
|
|
XM_017009179.2:c.8119G=
|
XP_016864668.1:p.Val2707=
|
|
XM_017009180.1:c.9214G=
|
XP_016864669.1:p.Val3072=
|
|
XM_017009181.1:c.9214G=
|
XP_016864670.1:p.Val3072=
|
|
XM_017009182.1:c.9214G=
|
XP_016864671.1:p.Val3072=
|
|
XM_017009183.1:c.9214G=
|
XP_016864672.1:p.Val3072=
|
|
XM_017009184.1:c.9209G=
|
XP_016864673.1:p.Gly3070=
|
|
XM_017009185.1:c.4303G=
|
XP_016864674.1:p.Val1435=
|
|
XM_017009186.1:c.3856G=
|
XP_016864675.1:p.Val1286=
|
|
XM_017009188.1:c.3193G=
|
XP_016864677.1:p.Val1065=
|
|
XM_024454388.1:c.8119G=
|
XP_024310156.1:p.Val2707=
|
|
XM_024454389.1:c.7708G=
|
XP_024310157.1:p.Val2570=
|
|
XR_001742034.1:n.9100G=
|
|
|
XR_001742035.1:n.9095G=
|
|
|
NM_001369.3:c.9106G=
MANE Select
|
NP_001360.1:p.Val3036=
|
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