ENST00000373344.11:c.7458T>G
MANE Select
|
ENSP00000362441.4:p.Pro2486=
|
|
ENST00000675732.1:c.2556T>G
|
ENSP00000502598.1:p.Pro852=
|
|
ENST00000373344.9:c.7458T>G
|
ENSP00000362441.4:p.Pro2486=
|
|
ENST00000395603.7:c.7344T>G
|
ENSP00000378967.3:p.Pro2448=
|
|
ENST00000480283.5:c.*7086T>G
|
ENSP00000480196.1:n.*7086T>G
|
|
ENST00000623706.3:n.5778T>G
|
|
|
NM_000489.4:c.7458T>G
|
NP_000480.3:p.Pro2486=
|
|
NM_138270.3:c.7344T>G
|
NP_612114.2:p.Pro2448=
|
|
XM_005262153.3:c.7455T>G
|
XP_005262210.2:p.Pro2485=
|
|
XM_005262154.3:c.7371T>G
|
XP_005262211.2:p.Pro2457=
|
|
XM_005262155.3:c.7341T>G
|
XP_005262212.2:p.Pro2447=
|
|
XM_005262156.3:c.7293T>G
|
XP_005262213.2:p.Pro2431=
|
|
XM_005262157.3:c.7254T>G
|
XP_005262214.2:p.Pro2418=
|
|
XM_006724666.2:c.7341T>G
|
XP_006724729.1:p.Pro2447=
|
|
XM_006724667.2:c.7179T>G
|
XP_006724730.1:p.Pro2393=
|
|
XR_938400.1:n.9050T>G
|
|
|
NM_000489.5:c.7458T>G
|
NP_000480.3:p.Pro2486=
|
|
XM_005262153.5:c.7455T>G
|
XP_005262210.2:p.Pro2485=
|
|
XM_005262154.5:c.7371T>G
|
XP_005262211.2:p.Pro2457=
|
|
XM_005262155.4:c.7341T>G
|
XP_005262212.2:p.Pro2447=
|
|
XM_005262156.4:c.7293T>G
|
XP_005262213.2:p.Pro2431=
|
|
XM_005262157.5:c.7254T>G
|
XP_005262214.2:p.Pro2418=
|
|
XM_006724666.4:c.7341T>G
|
XP_006724729.1:p.Pro2447=
|
|
XM_006724667.3:c.7179T>G
|
XP_006724730.1:p.Pro2393=
|
|
XM_017029601.2:c.7368T>G
|
XP_016885090.1:p.Pro2456=
|
|
XM_017029602.1:c.7338T>G
|
XP_016885091.1:p.Pro2446=
|
|
XM_017029603.1:c.7290T>G
|
XP_016885092.1:p.Pro2430=
|
|
XM_017029604.2:c.7257T>G
|
XP_016885093.1:p.Pro2419=
|
|
XM_017029605.1:c.7254T>G
|
XP_016885094.1:p.Pro2418=
|
|
XM_017029606.2:c.7227T>G
|
XP_016885095.1:p.Pro2409=
|
|
XM_017029607.2:c.7224T>G
|
XP_016885096.1:p.Pro2408=
|
|
XM_017029608.2:c.7176T>G
|
XP_016885097.1:p.Pro2392=
|
|
XM_017029609.1:c.7140T>G
|
XP_016885098.1:p.Pro2380=
|
|
XM_017029610.1:c.7137T>G
|
XP_016885099.1:p.Pro2379=
|
|
XM_017029611.1:c.7092T>G
|
XP_016885100.1:p.Pro2364=
|
|
XR_001755700.2:n.7757T>G
|
|
|
NM_138270.4:c.7344T>G
|
NP_612114.2:p.Pro2448=
|
|
NM_000489.6:c.7458T>G
MANE Select
|
NP_000480.3:p.Pro2486=
|
|
NM_138270.5:c.7344T>G
|
NP_612114.2:p.Pro2448=
|
|