ENST00000373344.11:c.7429C>T
MANE Select
|
ENSP00000362441.4:p.Pro2477Ser
|
|
ENST00000675732.1:c.2527C>T
|
ENSP00000502598.1:p.Pro843Ser
|
|
ENST00000373344.9:c.7429C>T
|
ENSP00000362441.4:p.Pro2477Ser
|
|
ENST00000395603.7:c.7315C>T
|
ENSP00000378967.3:p.Pro2439Ser
|
|
ENST00000480283.5:c.*7057C>T
|
ENSP00000480196.1:n.*7057C>T
|
|
ENST00000623706.3:n.5749C>T
|
|
|
NM_000489.4:c.7429C>T
|
NP_000480.3:p.Pro2477Ser
|
|
NM_138270.3:c.7315C>T
|
NP_612114.2:p.Pro2439Ser
|
|
XM_005262153.3:c.7426C>T
|
XP_005262210.2:p.Pro2476Ser
|
|
XM_005262154.3:c.7342C>T
|
XP_005262211.2:p.Pro2448Ser
|
|
XM_005262155.3:c.7312C>T
|
XP_005262212.2:p.Pro2438Ser
|
|
XM_005262156.3:c.7264C>T
|
XP_005262213.2:p.Pro2422Ser
|
|
XM_005262157.3:c.7225C>T
|
XP_005262214.2:p.Pro2409Ser
|
|
XM_006724666.2:c.7312C>T
|
XP_006724729.1:p.Pro2438Ser
|
|
XM_006724667.2:c.7150C>T
|
XP_006724730.1:p.Pro2384Ser
|
|
XR_938400.1:n.9021C>T
|
|
|
NM_000489.5:c.7429C>T
|
NP_000480.3:p.Pro2477Ser
|
|
XM_005262153.5:c.7426C>T
|
XP_005262210.2:p.Pro2476Ser
|
|
XM_005262154.5:c.7342C>T
|
XP_005262211.2:p.Pro2448Ser
|
|
XM_005262155.4:c.7312C>T
|
XP_005262212.2:p.Pro2438Ser
|
|
XM_005262156.4:c.7264C>T
|
XP_005262213.2:p.Pro2422Ser
|
|
XM_005262157.5:c.7225C>T
|
XP_005262214.2:p.Pro2409Ser
|
|
XM_006724666.4:c.7312C>T
|
XP_006724729.1:p.Pro2438Ser
|
|
XM_006724667.3:c.7150C>T
|
XP_006724730.1:p.Pro2384Ser
|
|
XM_017029601.2:c.7339C>T
|
XP_016885090.1:p.Pro2447Ser
|
|
XM_017029602.1:c.7309C>T
|
XP_016885091.1:p.Pro2437Ser
|
|
XM_017029603.1:c.7261C>T
|
XP_016885092.1:p.Pro2421Ser
|
|
XM_017029604.2:c.7228C>T
|
XP_016885093.1:p.Pro2410Ser
|
|
XM_017029605.1:c.7225C>T
|
XP_016885094.1:p.Pro2409Ser
|
|
XM_017029606.2:c.7198C>T
|
XP_016885095.1:p.Pro2400Ser
|
|
XM_017029607.2:c.7195C>T
|
XP_016885096.1:p.Pro2399Ser
|
|
XM_017029608.2:c.7147C>T
|
XP_016885097.1:p.Pro2383Ser
|
|
XM_017029609.1:c.7111C>T
|
XP_016885098.1:p.Pro2371Ser
|
|
XM_017029610.1:c.7108C>T
|
XP_016885099.1:p.Pro2370Ser
|
|
XM_017029611.1:c.7063C>T
|
XP_016885100.1:p.Pro2355Ser
|
|
XR_001755700.2:n.7728C>T
|
|
|
NM_138270.4:c.7315C>T
|
NP_612114.2:p.Pro2439Ser
|
|
NM_000489.6:c.7429C>T
MANE Select
|
NP_000480.3:p.Pro2477Ser
|
|
NM_138270.5:c.7315C>T
|
NP_612114.2:p.Pro2439Ser
|
|