ENST00000373344.11:c.7281T>A
MANE Select
|
ENSP00000362441.4:p.Thr2427=
|
|
ENST00000675732.1:c.2379T>A
|
ENSP00000502598.1:p.Thr793=
|
|
ENST00000373344.9:c.7281T>A
|
ENSP00000362441.4:p.Thr2427=
|
|
ENST00000395603.7:c.7167T>A
|
ENSP00000378967.3:p.Thr2389=
|
|
ENST00000480283.5:c.*6909T>A
|
ENSP00000480196.1:n.*6909T>A
|
|
ENST00000623706.3:n.5601T>A
|
|
|
ENST00000624766.1:n.512T>A
|
|
|
NM_000489.4:c.7281T>A
|
NP_000480.3:p.Thr2427=
|
|
NM_138270.3:c.7167T>A
|
NP_612114.2:p.Thr2389=
|
|
XM_005262153.3:c.7278T>A
|
XP_005262210.2:p.Thr2426=
|
|
XM_005262154.3:c.7194T>A
|
XP_005262211.2:p.Thr2398=
|
|
XM_005262155.3:c.7164T>A
|
XP_005262212.2:p.Thr2388=
|
|
XM_005262156.3:c.7116T>A
|
XP_005262213.2:p.Thr2372=
|
|
XM_005262157.3:c.7077T>A
|
XP_005262214.2:p.Thr2359=
|
|
XM_006724666.2:c.7164T>A
|
XP_006724729.1:p.Thr2388=
|
|
XM_006724667.2:c.7002T>A
|
XP_006724730.1:p.Thr2334=
|
|
XR_938400.1:n.8873T>A
|
|
|
NM_000489.5:c.7281T>A
|
NP_000480.3:p.Thr2427=
|
|
XM_005262153.5:c.7278T>A
|
XP_005262210.2:p.Thr2426=
|
|
XM_005262154.5:c.7194T>A
|
XP_005262211.2:p.Thr2398=
|
|
XM_005262155.4:c.7164T>A
|
XP_005262212.2:p.Thr2388=
|
|
XM_005262156.4:c.7116T>A
|
XP_005262213.2:p.Thr2372=
|
|
XM_005262157.5:c.7077T>A
|
XP_005262214.2:p.Thr2359=
|
|
XM_006724666.4:c.7164T>A
|
XP_006724729.1:p.Thr2388=
|
|
XM_006724667.3:c.7002T>A
|
XP_006724730.1:p.Thr2334=
|
|
XM_017029601.2:c.7191T>A
|
XP_016885090.1:p.Thr2397=
|
|
XM_017029602.1:c.7161T>A
|
XP_016885091.1:p.Thr2387=
|
|
XM_017029603.1:c.7113T>A
|
XP_016885092.1:p.Thr2371=
|
|
XM_017029604.2:c.7080T>A
|
XP_016885093.1:p.Thr2360=
|
|
XM_017029605.1:c.7077T>A
|
XP_016885094.1:p.Thr2359=
|
|
XM_017029606.2:c.7050T>A
|
XP_016885095.1:p.Thr2350=
|
|
XM_017029607.2:c.7047T>A
|
XP_016885096.1:p.Thr2349=
|
|
XM_017029608.2:c.6999T>A
|
XP_016885097.1:p.Thr2333=
|
|
XM_017029609.1:c.6963T>A
|
XP_016885098.1:p.Thr2321=
|
|
XM_017029610.1:c.6960T>A
|
XP_016885099.1:p.Thr2320=
|
|
XM_017029611.1:c.6915T>A
|
XP_016885100.1:p.Thr2305=
|
|
XR_001755700.2:n.7580T>A
|
|
|
NM_138270.4:c.7167T>A
|
NP_612114.2:p.Thr2389=
|
|
NM_000489.6:c.7281T>A
MANE Select
|
NP_000480.3:p.Thr2427=
|
|
NM_138270.5:c.7167T>A
|
NP_612114.2:p.Thr2389=
|
|