ENST00000373344.11:c.7447A>T
MANE Select
|
ENSP00000362441.4:p.Asn2483Tyr
|
|
ENST00000675732.1:c.2545A>T
|
ENSP00000502598.1:p.Asn849Tyr
|
|
ENST00000373344.9:c.7447A>T
|
ENSP00000362441.4:p.Asn2483Tyr
|
|
ENST00000395603.7:c.7333A>T
|
ENSP00000378967.3:p.Asn2445Tyr
|
|
ENST00000480283.5:c.*7075A>T
|
ENSP00000480196.1:n.*7075A>T
|
|
ENST00000623706.3:n.5767A>T
|
|
|
NM_000489.4:c.7447A>T
|
NP_000480.3:p.Asn2483Tyr
|
|
NM_138270.3:c.7333A>T
|
NP_612114.2:p.Asn2445Tyr
|
|
XM_005262153.3:c.7444A>T
|
XP_005262210.2:p.Asn2482Tyr
|
|
XM_005262154.3:c.7360A>T
|
XP_005262211.2:p.Asn2454Tyr
|
|
XM_005262155.3:c.7330A>T
|
XP_005262212.2:p.Asn2444Tyr
|
|
XM_005262156.3:c.7282A>T
|
XP_005262213.2:p.Asn2428Tyr
|
|
XM_005262157.3:c.7243A>T
|
XP_005262214.2:p.Asn2415Tyr
|
|
XM_006724666.2:c.7330A>T
|
XP_006724729.1:p.Asn2444Tyr
|
|
XM_006724667.2:c.7168A>T
|
XP_006724730.1:p.Asn2390Tyr
|
|
XR_938400.1:n.9039A>T
|
|
|
NM_000489.5:c.7447A>T
|
NP_000480.3:p.Asn2483Tyr
|
|
XM_005262153.5:c.7444A>T
|
XP_005262210.2:p.Asn2482Tyr
|
|
XM_005262154.5:c.7360A>T
|
XP_005262211.2:p.Asn2454Tyr
|
|
XM_005262155.4:c.7330A>T
|
XP_005262212.2:p.Asn2444Tyr
|
|
XM_005262156.4:c.7282A>T
|
XP_005262213.2:p.Asn2428Tyr
|
|
XM_005262157.5:c.7243A>T
|
XP_005262214.2:p.Asn2415Tyr
|
|
XM_006724666.4:c.7330A>T
|
XP_006724729.1:p.Asn2444Tyr
|
|
XM_006724667.3:c.7168A>T
|
XP_006724730.1:p.Asn2390Tyr
|
|
XM_017029601.2:c.7357A>T
|
XP_016885090.1:p.Asn2453Tyr
|
|
XM_017029602.1:c.7327A>T
|
XP_016885091.1:p.Asn2443Tyr
|
|
XM_017029603.1:c.7279A>T
|
XP_016885092.1:p.Asn2427Tyr
|
|
XM_017029604.2:c.7246A>T
|
XP_016885093.1:p.Asn2416Tyr
|
|
XM_017029605.1:c.7243A>T
|
XP_016885094.1:p.Asn2415Tyr
|
|
XM_017029606.2:c.7216A>T
|
XP_016885095.1:p.Asn2406Tyr
|
|
XM_017029607.2:c.7213A>T
|
XP_016885096.1:p.Asn2405Tyr
|
|
XM_017029608.2:c.7165A>T
|
XP_016885097.1:p.Asn2389Tyr
|
|
XM_017029609.1:c.7129A>T
|
XP_016885098.1:p.Asn2377Tyr
|
|
XM_017029610.1:c.7126A>T
|
XP_016885099.1:p.Asn2376Tyr
|
|
XM_017029611.1:c.7081A>T
|
XP_016885100.1:p.Asn2361Tyr
|
|
XR_001755700.2:n.7746A>T
|
|
|
NM_138270.4:c.7333A>T
|
NP_612114.2:p.Asn2445Tyr
|
|
NM_000489.6:c.7447A>T
MANE Select
|
NP_000480.3:p.Asn2483Tyr
|
|
NM_138270.5:c.7333A>T
|
NP_612114.2:p.Asn2445Tyr
|
|