ENST00000373344.11:c.4453A>T
MANE Select
|
ENSP00000362441.4:p.Lys1485Ter
|
|
ENST00000373344.9:c.4453A>T
|
ENSP00000362441.4:p.Lys1485Ter
|
|
ENST00000395603.7:c.4339A>T
|
ENSP00000378967.3:p.Lys1447Ter
|
|
ENST00000480283.5:c.*4081A>T
|
ENSP00000480196.1:n.*4081A>T
|
|
ENST00000623242.3:c.59A>T
|
|
|
NM_000489.4:c.4453A>T
|
NP_000480.3:p.Lys1485Ter
|
|
NM_138270.3:c.4339A>T
|
NP_612114.2:p.Lys1447Ter
|
|
XM_005262153.3:c.4450A>T
|
XP_005262210.2:p.Lys1484Ter
|
|
XM_005262154.3:c.4366A>T
|
XP_005262211.2:p.Lys1456Ter
|
|
XM_005262155.3:c.4336A>T
|
XP_005262212.2:p.Lys1446Ter
|
|
XM_005262156.3:c.4288A>T
|
XP_005262213.2:p.Lys1430Ter
|
|
XM_005262157.3:c.4249A>T
|
XP_005262214.2:p.Lys1417Ter
|
|
XM_006724666.2:c.4336A>T
|
XP_006724729.1:p.Lys1446Ter
|
|
XM_006724667.2:c.4174A>T
|
XP_006724730.1:p.Lys1392Ter
|
|
XM_006724668.2:c.4453A>T
|
XP_006724731.1:p.Lys1485Ter
|
|
XR_938400.1:n.4721A>T
|
|
|
NM_000489.5:c.4453A>T
|
NP_000480.3:p.Lys1485Ter
|
|
XM_005262153.5:c.4450A>T
|
XP_005262210.2:p.Lys1484Ter
|
|
XM_005262154.5:c.4366A>T
|
XP_005262211.2:p.Lys1456Ter
|
|
XM_005262155.4:c.4336A>T
|
XP_005262212.2:p.Lys1446Ter
|
|
XM_005262156.4:c.4288A>T
|
XP_005262213.2:p.Lys1430Ter
|
|
XM_005262157.5:c.4249A>T
|
XP_005262214.2:p.Lys1417Ter
|
|
XM_006724666.4:c.4336A>T
|
XP_006724729.1:p.Lys1446Ter
|
|
XM_006724667.3:c.4174A>T
|
XP_006724730.1:p.Lys1392Ter
|
|
XM_006724668.3:c.4453A>T
|
XP_006724731.1:p.Lys1485Ter
|
|
XM_017029601.2:c.4363A>T
|
XP_016885090.1:p.Lys1455Ter
|
|
XM_017029602.1:c.4333A>T
|
XP_016885091.1:p.Lys1445Ter
|
|
XM_017029603.1:c.4285A>T
|
XP_016885092.1:p.Lys1429Ter
|
|
XM_017029604.2:c.4252A>T
|
XP_016885093.1:p.Lys1418Ter
|
|
XM_017029605.1:c.4249A>T
|
XP_016885094.1:p.Lys1417Ter
|
|
XM_017029606.2:c.4222A>T
|
XP_016885095.1:p.Lys1408Ter
|
|
XM_017029607.2:c.4219A>T
|
XP_016885096.1:p.Lys1407Ter
|
|
XM_017029608.2:c.4171A>T
|
XP_016885097.1:p.Lys1391Ter
|
|
XM_017029609.1:c.4135A>T
|
XP_016885098.1:p.Lys1379Ter
|
|
XM_017029610.1:c.4132A>T
|
XP_016885099.1:p.Lys1378Ter
|
|
XM_017029611.1:c.4087A>T
|
XP_016885100.1:p.Lys1363Ter
|
|
XR_001755700.2:n.4678A>T
|
|
|
NM_138270.4:c.4339A>T
|
NP_612114.2:p.Lys1447Ter
|
|
NM_000489.6:c.4453A>T
MANE Select
|
NP_000480.3:p.Lys1485Ter
|
|
NM_138270.5:c.4339A>T
|
NP_612114.2:p.Lys1447Ter
|
|