ENST00000373344.11:c.7280C>A
MANE Select
|
ENSP00000362441.4:p.Thr2427Asn
|
|
ENST00000675732.1:c.2378C>A
|
ENSP00000502598.1:p.Thr793Asn
|
|
ENST00000373344.9:c.7280C>A
|
ENSP00000362441.4:p.Thr2427Asn
|
|
ENST00000395603.7:c.7166C>A
|
ENSP00000378967.3:p.Thr2389Asn
|
|
ENST00000480283.5:c.*6908C>A
|
ENSP00000480196.1:n.*6908C>A
|
|
ENST00000623706.3:n.5600C>A
|
|
|
ENST00000624766.1:n.511C>A
|
|
|
NM_000489.4:c.7280C>A
|
NP_000480.3:p.Thr2427Asn
|
|
NM_138270.3:c.7166C>A
|
NP_612114.2:p.Thr2389Asn
|
|
XM_005262153.3:c.7277C>A
|
XP_005262210.2:p.Thr2426Asn
|
|
XM_005262154.3:c.7193C>A
|
XP_005262211.2:p.Thr2398Asn
|
|
XM_005262155.3:c.7163C>A
|
XP_005262212.2:p.Thr2388Asn
|
|
XM_005262156.3:c.7115C>A
|
XP_005262213.2:p.Thr2372Asn
|
|
XM_005262157.3:c.7076C>A
|
XP_005262214.2:p.Thr2359Asn
|
|
XM_006724666.2:c.7163C>A
|
XP_006724729.1:p.Thr2388Asn
|
|
XM_006724667.2:c.7001C>A
|
XP_006724730.1:p.Thr2334Asn
|
|
XR_938400.1:n.8872C>A
|
|
|
NM_000489.5:c.7280C>A
|
NP_000480.3:p.Thr2427Asn
|
|
XM_005262153.5:c.7277C>A
|
XP_005262210.2:p.Thr2426Asn
|
|
XM_005262154.5:c.7193C>A
|
XP_005262211.2:p.Thr2398Asn
|
|
XM_005262155.4:c.7163C>A
|
XP_005262212.2:p.Thr2388Asn
|
|
XM_005262156.4:c.7115C>A
|
XP_005262213.2:p.Thr2372Asn
|
|
XM_005262157.5:c.7076C>A
|
XP_005262214.2:p.Thr2359Asn
|
|
XM_006724666.4:c.7163C>A
|
XP_006724729.1:p.Thr2388Asn
|
|
XM_006724667.3:c.7001C>A
|
XP_006724730.1:p.Thr2334Asn
|
|
XM_017029601.2:c.7190C>A
|
XP_016885090.1:p.Thr2397Asn
|
|
XM_017029602.1:c.7160C>A
|
XP_016885091.1:p.Thr2387Asn
|
|
XM_017029603.1:c.7112C>A
|
XP_016885092.1:p.Thr2371Asn
|
|
XM_017029604.2:c.7079C>A
|
XP_016885093.1:p.Thr2360Asn
|
|
XM_017029605.1:c.7076C>A
|
XP_016885094.1:p.Thr2359Asn
|
|
XM_017029606.2:c.7049C>A
|
XP_016885095.1:p.Thr2350Asn
|
|
XM_017029607.2:c.7046C>A
|
XP_016885096.1:p.Thr2349Asn
|
|
XM_017029608.2:c.6998C>A
|
XP_016885097.1:p.Thr2333Asn
|
|
XM_017029609.1:c.6962C>A
|
XP_016885098.1:p.Thr2321Asn
|
|
XM_017029610.1:c.6959C>A
|
XP_016885099.1:p.Thr2320Asn
|
|
XM_017029611.1:c.6914C>A
|
XP_016885100.1:p.Thr2305Asn
|
|
XR_001755700.2:n.7579C>A
|
|
|
NM_138270.4:c.7166C>A
|
NP_612114.2:p.Thr2389Asn
|
|
NM_000489.6:c.7280C>A
MANE Select
|
NP_000480.3:p.Thr2427Asn
|
|
NM_138270.5:c.7166C>A
|
NP_612114.2:p.Thr2389Asn
|
|