ENST00000373344.11:c.7347T>A
MANE Select
|
ENSP00000362441.4:p.Ser2449=
|
|
ENST00000675732.1:c.2445T>A
|
ENSP00000502598.1:p.Ser815=
|
|
ENST00000373344.9:c.7347T>A
|
ENSP00000362441.4:p.Ser2449=
|
|
ENST00000395603.7:c.7233T>A
|
ENSP00000378967.3:p.Ser2411=
|
|
ENST00000480283.5:c.*6975T>A
|
ENSP00000480196.1:n.*6975T>A
|
|
ENST00000623706.3:n.5667T>A
|
|
|
ENST00000624766.1:n.578T>A
|
|
|
NM_000489.4:c.7347T>A
|
NP_000480.3:p.Ser2449=
|
|
NM_138270.3:c.7233T>A
|
NP_612114.2:p.Ser2411=
|
|
XM_005262153.3:c.7344T>A
|
XP_005262210.2:p.Ser2448=
|
|
XM_005262154.3:c.7260T>A
|
XP_005262211.2:p.Ser2420=
|
|
XM_005262155.3:c.7230T>A
|
XP_005262212.2:p.Ser2410=
|
|
XM_005262156.3:c.7182T>A
|
XP_005262213.2:p.Ser2394=
|
|
XM_005262157.3:c.7143T>A
|
XP_005262214.2:p.Ser2381=
|
|
XM_006724666.2:c.7230T>A
|
XP_006724729.1:p.Ser2410=
|
|
XM_006724667.2:c.7068T>A
|
XP_006724730.1:p.Ser2356=
|
|
XR_938400.1:n.8939T>A
|
|
|
NM_000489.5:c.7347T>A
|
NP_000480.3:p.Ser2449=
|
|
XM_005262153.5:c.7344T>A
|
XP_005262210.2:p.Ser2448=
|
|
XM_005262154.5:c.7260T>A
|
XP_005262211.2:p.Ser2420=
|
|
XM_005262155.4:c.7230T>A
|
XP_005262212.2:p.Ser2410=
|
|
XM_005262156.4:c.7182T>A
|
XP_005262213.2:p.Ser2394=
|
|
XM_005262157.5:c.7143T>A
|
XP_005262214.2:p.Ser2381=
|
|
XM_006724666.4:c.7230T>A
|
XP_006724729.1:p.Ser2410=
|
|
XM_006724667.3:c.7068T>A
|
XP_006724730.1:p.Ser2356=
|
|
XM_017029601.2:c.7257T>A
|
XP_016885090.1:p.Ser2419=
|
|
XM_017029602.1:c.7227T>A
|
XP_016885091.1:p.Ser2409=
|
|
XM_017029603.1:c.7179T>A
|
XP_016885092.1:p.Ser2393=
|
|
XM_017029604.2:c.7146T>A
|
XP_016885093.1:p.Ser2382=
|
|
XM_017029605.1:c.7143T>A
|
XP_016885094.1:p.Ser2381=
|
|
XM_017029606.2:c.7116T>A
|
XP_016885095.1:p.Ser2372=
|
|
XM_017029607.2:c.7113T>A
|
XP_016885096.1:p.Ser2371=
|
|
XM_017029608.2:c.7065T>A
|
XP_016885097.1:p.Ser2355=
|
|
XM_017029609.1:c.7029T>A
|
XP_016885098.1:p.Ser2343=
|
|
XM_017029610.1:c.7026T>A
|
XP_016885099.1:p.Ser2342=
|
|
XM_017029611.1:c.6981T>A
|
XP_016885100.1:p.Ser2327=
|
|
XR_001755700.2:n.7646T>A
|
|
|
NM_138270.4:c.7233T>A
|
NP_612114.2:p.Ser2411=
|
|
NM_000489.6:c.7347T>A
MANE Select
|
NP_000480.3:p.Ser2449=
|
|
NM_138270.5:c.7233T>A
|
NP_612114.2:p.Ser2411=
|
|