ENST00000373344.11:c.7353C>A
MANE Select
|
ENSP00000362441.4:p.Tyr2451Ter
|
|
ENST00000675732.1:c.2451C>A
|
ENSP00000502598.1:p.Tyr817Ter
|
|
ENST00000373344.9:c.7353C>A
|
ENSP00000362441.4:p.Tyr2451Ter
|
|
ENST00000395603.7:c.7239C>A
|
ENSP00000378967.3:p.Tyr2413Ter
|
|
ENST00000480283.5:c.*6981C>A
|
ENSP00000480196.1:n.*6981C>A
|
|
ENST00000623706.3:n.5673C>A
|
|
|
NM_000489.4:c.7353C>A
|
NP_000480.3:p.Tyr2451Ter
|
|
NM_138270.3:c.7239C>A
|
NP_612114.2:p.Tyr2413Ter
|
|
XM_005262153.3:c.7350C>A
|
XP_005262210.2:p.Tyr2450Ter
|
|
XM_005262154.3:c.7266C>A
|
XP_005262211.2:p.Tyr2422Ter
|
|
XM_005262155.3:c.7236C>A
|
XP_005262212.2:p.Tyr2412Ter
|
|
XM_005262156.3:c.7188C>A
|
XP_005262213.2:p.Tyr2396Ter
|
|
XM_005262157.3:c.7149C>A
|
XP_005262214.2:p.Tyr2383Ter
|
|
XM_006724666.2:c.7236C>A
|
XP_006724729.1:p.Tyr2412Ter
|
|
XM_006724667.2:c.7074C>A
|
XP_006724730.1:p.Tyr2358Ter
|
|
XR_938400.1:n.8945C>A
|
|
|
NM_000489.5:c.7353C>A
|
NP_000480.3:p.Tyr2451Ter
|
|
XM_005262153.5:c.7350C>A
|
XP_005262210.2:p.Tyr2450Ter
|
|
XM_005262154.5:c.7266C>A
|
XP_005262211.2:p.Tyr2422Ter
|
|
XM_005262155.4:c.7236C>A
|
XP_005262212.2:p.Tyr2412Ter
|
|
XM_005262156.4:c.7188C>A
|
XP_005262213.2:p.Tyr2396Ter
|
|
XM_005262157.5:c.7149C>A
|
XP_005262214.2:p.Tyr2383Ter
|
|
XM_006724666.4:c.7236C>A
|
XP_006724729.1:p.Tyr2412Ter
|
|
XM_006724667.3:c.7074C>A
|
XP_006724730.1:p.Tyr2358Ter
|
|
XM_017029601.2:c.7263C>A
|
XP_016885090.1:p.Tyr2421Ter
|
|
XM_017029602.1:c.7233C>A
|
XP_016885091.1:p.Tyr2411Ter
|
|
XM_017029603.1:c.7185C>A
|
XP_016885092.1:p.Tyr2395Ter
|
|
XM_017029604.2:c.7152C>A
|
XP_016885093.1:p.Tyr2384Ter
|
|
XM_017029605.1:c.7149C>A
|
XP_016885094.1:p.Tyr2383Ter
|
|
XM_017029606.2:c.7122C>A
|
XP_016885095.1:p.Tyr2374Ter
|
|
XM_017029607.2:c.7119C>A
|
XP_016885096.1:p.Tyr2373Ter
|
|
XM_017029608.2:c.7071C>A
|
XP_016885097.1:p.Tyr2357Ter
|
|
XM_017029609.1:c.7035C>A
|
XP_016885098.1:p.Tyr2345Ter
|
|
XM_017029610.1:c.7032C>A
|
XP_016885099.1:p.Tyr2344Ter
|
|
XM_017029611.1:c.6987C>A
|
XP_016885100.1:p.Tyr2329Ter
|
|
XR_001755700.2:n.7652C>A
|
|
|
NM_138270.4:c.7239C>A
|
NP_612114.2:p.Tyr2413Ter
|
|
NM_000489.6:c.7353C>A
MANE Select
|
NP_000480.3:p.Tyr2451Ter
|
|
NM_138270.5:c.7239C>A
|
NP_612114.2:p.Tyr2413Ter
|
|