ENST00000373344.11:c.7433C>A
MANE Select
|
ENSP00000362441.4:p.Pro2478Gln
|
|
ENST00000675732.1:c.2531C>A
|
ENSP00000502598.1:p.Pro844Gln
|
|
ENST00000373344.9:c.7433C>A
|
ENSP00000362441.4:p.Pro2478Gln
|
|
ENST00000395603.7:c.7319C>A
|
ENSP00000378967.3:p.Pro2440Gln
|
|
ENST00000480283.5:c.*7061C>A
|
ENSP00000480196.1:n.*7061C>A
|
|
ENST00000623706.3:n.5753C>A
|
|
|
NM_000489.4:c.7433C>A
|
NP_000480.3:p.Pro2478Gln
|
|
NM_138270.3:c.7319C>A
|
NP_612114.2:p.Pro2440Gln
|
|
XM_005262153.3:c.7430C>A
|
XP_005262210.2:p.Pro2477Gln
|
|
XM_005262154.3:c.7346C>A
|
XP_005262211.2:p.Pro2449Gln
|
|
XM_005262155.3:c.7316C>A
|
XP_005262212.2:p.Pro2439Gln
|
|
XM_005262156.3:c.7268C>A
|
XP_005262213.2:p.Pro2423Gln
|
|
XM_005262157.3:c.7229C>A
|
XP_005262214.2:p.Pro2410Gln
|
|
XM_006724666.2:c.7316C>A
|
XP_006724729.1:p.Pro2439Gln
|
|
XM_006724667.2:c.7154C>A
|
XP_006724730.1:p.Pro2385Gln
|
|
XR_938400.1:n.9025C>A
|
|
|
NM_000489.5:c.7433C>A
|
NP_000480.3:p.Pro2478Gln
|
|
XM_005262153.5:c.7430C>A
|
XP_005262210.2:p.Pro2477Gln
|
|
XM_005262154.5:c.7346C>A
|
XP_005262211.2:p.Pro2449Gln
|
|
XM_005262155.4:c.7316C>A
|
XP_005262212.2:p.Pro2439Gln
|
|
XM_005262156.4:c.7268C>A
|
XP_005262213.2:p.Pro2423Gln
|
|
XM_005262157.5:c.7229C>A
|
XP_005262214.2:p.Pro2410Gln
|
|
XM_006724666.4:c.7316C>A
|
XP_006724729.1:p.Pro2439Gln
|
|
XM_006724667.3:c.7154C>A
|
XP_006724730.1:p.Pro2385Gln
|
|
XM_017029601.2:c.7343C>A
|
XP_016885090.1:p.Pro2448Gln
|
|
XM_017029602.1:c.7313C>A
|
XP_016885091.1:p.Pro2438Gln
|
|
XM_017029603.1:c.7265C>A
|
XP_016885092.1:p.Pro2422Gln
|
|
XM_017029604.2:c.7232C>A
|
XP_016885093.1:p.Pro2411Gln
|
|
XM_017029605.1:c.7229C>A
|
XP_016885094.1:p.Pro2410Gln
|
|
XM_017029606.2:c.7202C>A
|
XP_016885095.1:p.Pro2401Gln
|
|
XM_017029607.2:c.7199C>A
|
XP_016885096.1:p.Pro2400Gln
|
|
XM_017029608.2:c.7151C>A
|
XP_016885097.1:p.Pro2384Gln
|
|
XM_017029609.1:c.7115C>A
|
XP_016885098.1:p.Pro2372Gln
|
|
XM_017029610.1:c.7112C>A
|
XP_016885099.1:p.Pro2371Gln
|
|
XM_017029611.1:c.7067C>A
|
XP_016885100.1:p.Pro2356Gln
|
|
XR_001755700.2:n.7732C>A
|
|
|
NM_138270.4:c.7319C>A
|
NP_612114.2:p.Pro2440Gln
|
|
NM_000489.6:c.7433C>A
MANE Select
|
NP_000480.3:p.Pro2478Gln
|
|
NM_138270.5:c.7319C>A
|
NP_612114.2:p.Pro2440Gln
|
|