ENST00000373344.11:c.7427C>T
MANE Select
|
ENSP00000362441.4:p.Pro2476Leu
|
|
ENST00000675732.1:c.2525C>T
|
ENSP00000502598.1:p.Pro842Leu
|
|
ENST00000373344.9:c.7427C>T
|
ENSP00000362441.4:p.Pro2476Leu
|
|
ENST00000395603.7:c.7313C>T
|
ENSP00000378967.3:p.Pro2438Leu
|
|
ENST00000480283.5:c.*7055C>T
|
ENSP00000480196.1:n.*7055C>T
|
|
ENST00000623706.3:n.5747C>T
|
|
|
NM_000489.4:c.7427C>T
|
NP_000480.3:p.Pro2476Leu
|
|
NM_138270.3:c.7313C>T
|
NP_612114.2:p.Pro2438Leu
|
|
XM_005262153.3:c.7424C>T
|
XP_005262210.2:p.Pro2475Leu
|
|
XM_005262154.3:c.7340C>T
|
XP_005262211.2:p.Pro2447Leu
|
|
XM_005262155.3:c.7310C>T
|
XP_005262212.2:p.Pro2437Leu
|
|
XM_005262156.3:c.7262C>T
|
XP_005262213.2:p.Pro2421Leu
|
|
XM_005262157.3:c.7223C>T
|
XP_005262214.2:p.Pro2408Leu
|
|
XM_006724666.2:c.7310C>T
|
XP_006724729.1:p.Pro2437Leu
|
|
XM_006724667.2:c.7148C>T
|
XP_006724730.1:p.Pro2383Leu
|
|
XR_938400.1:n.9019C>T
|
|
|
NM_000489.5:c.7427C>T
|
NP_000480.3:p.Pro2476Leu
|
|
XM_005262153.5:c.7424C>T
|
XP_005262210.2:p.Pro2475Leu
|
|
XM_005262154.5:c.7340C>T
|
XP_005262211.2:p.Pro2447Leu
|
|
XM_005262155.4:c.7310C>T
|
XP_005262212.2:p.Pro2437Leu
|
|
XM_005262156.4:c.7262C>T
|
XP_005262213.2:p.Pro2421Leu
|
|
XM_005262157.5:c.7223C>T
|
XP_005262214.2:p.Pro2408Leu
|
|
XM_006724666.4:c.7310C>T
|
XP_006724729.1:p.Pro2437Leu
|
|
XM_006724667.3:c.7148C>T
|
XP_006724730.1:p.Pro2383Leu
|
|
XM_017029601.2:c.7337C>T
|
XP_016885090.1:p.Pro2446Leu
|
|
XM_017029602.1:c.7307C>T
|
XP_016885091.1:p.Pro2436Leu
|
|
XM_017029603.1:c.7259C>T
|
XP_016885092.1:p.Pro2420Leu
|
|
XM_017029604.2:c.7226C>T
|
XP_016885093.1:p.Pro2409Leu
|
|
XM_017029605.1:c.7223C>T
|
XP_016885094.1:p.Pro2408Leu
|
|
XM_017029606.2:c.7196C>T
|
XP_016885095.1:p.Pro2399Leu
|
|
XM_017029607.2:c.7193C>T
|
XP_016885096.1:p.Pro2398Leu
|
|
XM_017029608.2:c.7145C>T
|
XP_016885097.1:p.Pro2382Leu
|
|
XM_017029609.1:c.7109C>T
|
XP_016885098.1:p.Pro2370Leu
|
|
XM_017029610.1:c.7106C>T
|
XP_016885099.1:p.Pro2369Leu
|
|
XM_017029611.1:c.7061C>T
|
XP_016885100.1:p.Pro2354Leu
|
|
XR_001755700.2:n.7726C>T
|
|
|
NM_138270.4:c.7313C>T
|
NP_612114.2:p.Pro2438Leu
|
|
NM_000489.6:c.7427C>T
MANE Select
|
NP_000480.3:p.Pro2476Leu
|
|
NM_138270.5:c.7313C>T
|
NP_612114.2:p.Pro2438Leu
|
|