ENST00000373344.11:c.7284T>G
MANE Select
|
ENSP00000362441.4:p.Tyr2428Ter
|
|
ENST00000675732.1:c.2382T>G
|
ENSP00000502598.1:p.Tyr794Ter
|
|
ENST00000373344.9:c.7284T>G
|
ENSP00000362441.4:p.Tyr2428Ter
|
|
ENST00000395603.7:c.7170T>G
|
ENSP00000378967.3:p.Tyr2390Ter
|
|
ENST00000480283.5:c.*6912T>G
|
ENSP00000480196.1:n.*6912T>G
|
|
ENST00000623706.3:n.5604T>G
|
|
|
ENST00000624766.1:n.515T>G
|
|
|
NM_000489.4:c.7284T>G
|
NP_000480.3:p.Tyr2428Ter
|
|
NM_138270.3:c.7170T>G
|
NP_612114.2:p.Tyr2390Ter
|
|
XM_005262153.3:c.7281T>G
|
XP_005262210.2:p.Tyr2427Ter
|
|
XM_005262154.3:c.7197T>G
|
XP_005262211.2:p.Tyr2399Ter
|
|
XM_005262155.3:c.7167T>G
|
XP_005262212.2:p.Tyr2389Ter
|
|
XM_005262156.3:c.7119T>G
|
XP_005262213.2:p.Tyr2373Ter
|
|
XM_005262157.3:c.7080T>G
|
XP_005262214.2:p.Tyr2360Ter
|
|
XM_006724666.2:c.7167T>G
|
XP_006724729.1:p.Tyr2389Ter
|
|
XM_006724667.2:c.7005T>G
|
XP_006724730.1:p.Tyr2335Ter
|
|
XR_938400.1:n.8876T>G
|
|
|
NM_000489.5:c.7284T>G
|
NP_000480.3:p.Tyr2428Ter
|
|
XM_005262153.5:c.7281T>G
|
XP_005262210.2:p.Tyr2427Ter
|
|
XM_005262154.5:c.7197T>G
|
XP_005262211.2:p.Tyr2399Ter
|
|
XM_005262155.4:c.7167T>G
|
XP_005262212.2:p.Tyr2389Ter
|
|
XM_005262156.4:c.7119T>G
|
XP_005262213.2:p.Tyr2373Ter
|
|
XM_005262157.5:c.7080T>G
|
XP_005262214.2:p.Tyr2360Ter
|
|
XM_006724666.4:c.7167T>G
|
XP_006724729.1:p.Tyr2389Ter
|
|
XM_006724667.3:c.7005T>G
|
XP_006724730.1:p.Tyr2335Ter
|
|
XM_017029601.2:c.7194T>G
|
XP_016885090.1:p.Tyr2398Ter
|
|
XM_017029602.1:c.7164T>G
|
XP_016885091.1:p.Tyr2388Ter
|
|
XM_017029603.1:c.7116T>G
|
XP_016885092.1:p.Tyr2372Ter
|
|
XM_017029604.2:c.7083T>G
|
XP_016885093.1:p.Tyr2361Ter
|
|
XM_017029605.1:c.7080T>G
|
XP_016885094.1:p.Tyr2360Ter
|
|
XM_017029606.2:c.7053T>G
|
XP_016885095.1:p.Tyr2351Ter
|
|
XM_017029607.2:c.7050T>G
|
XP_016885096.1:p.Tyr2350Ter
|
|
XM_017029608.2:c.7002T>G
|
XP_016885097.1:p.Tyr2334Ter
|
|
XM_017029609.1:c.6966T>G
|
XP_016885098.1:p.Tyr2322Ter
|
|
XM_017029610.1:c.6963T>G
|
XP_016885099.1:p.Tyr2321Ter
|
|
XM_017029611.1:c.6918T>G
|
XP_016885100.1:p.Tyr2306Ter
|
|
XR_001755700.2:n.7583T>G
|
|
|
NM_138270.4:c.7170T>G
|
NP_612114.2:p.Tyr2390Ter
|
|
NM_000489.6:c.7284T>G
MANE Select
|
NP_000480.3:p.Tyr2428Ter
|
|
NM_138270.5:c.7170T>G
|
NP_612114.2:p.Tyr2390Ter
|
|