ENST00000373344.11:c.7375A>C
MANE Select
|
ENSP00000362441.4:p.Met2459Leu
|
|
ENST00000675732.1:c.2473A>C
|
ENSP00000502598.1:p.Met825Leu
|
|
ENST00000373344.9:c.7375A>C
|
ENSP00000362441.4:p.Met2459Leu
|
|
ENST00000395603.7:c.7261A>C
|
ENSP00000378967.3:p.Met2421Leu
|
|
ENST00000480283.5:c.*7003A>C
|
ENSP00000480196.1:n.*7003A>C
|
|
ENST00000623706.3:n.5695A>C
|
|
|
NM_000489.4:c.7375A>C
|
NP_000480.3:p.Met2459Leu
|
|
NM_138270.3:c.7261A>C
|
NP_612114.2:p.Met2421Leu
|
|
XM_005262153.3:c.7372A>C
|
XP_005262210.2:p.Met2458Leu
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|
XM_005262154.3:c.7288A>C
|
XP_005262211.2:p.Met2430Leu
|
|
XM_005262155.3:c.7258A>C
|
XP_005262212.2:p.Met2420Leu
|
|
XM_005262156.3:c.7210A>C
|
XP_005262213.2:p.Met2404Leu
|
|
XM_005262157.3:c.7171A>C
|
XP_005262214.2:p.Met2391Leu
|
|
XM_006724666.2:c.7258A>C
|
XP_006724729.1:p.Met2420Leu
|
|
XM_006724667.2:c.7096A>C
|
XP_006724730.1:p.Met2366Leu
|
|
XR_938400.1:n.8967A>C
|
|
|
NM_000489.5:c.7375A>C
|
NP_000480.3:p.Met2459Leu
|
|
XM_005262153.5:c.7372A>C
|
XP_005262210.2:p.Met2458Leu
|
|
XM_005262154.5:c.7288A>C
|
XP_005262211.2:p.Met2430Leu
|
|
XM_005262155.4:c.7258A>C
|
XP_005262212.2:p.Met2420Leu
|
|
XM_005262156.4:c.7210A>C
|
XP_005262213.2:p.Met2404Leu
|
|
XM_005262157.5:c.7171A>C
|
XP_005262214.2:p.Met2391Leu
|
|
XM_006724666.4:c.7258A>C
|
XP_006724729.1:p.Met2420Leu
|
|
XM_006724667.3:c.7096A>C
|
XP_006724730.1:p.Met2366Leu
|
|
XM_017029601.2:c.7285A>C
|
XP_016885090.1:p.Met2429Leu
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|
XM_017029602.1:c.7255A>C
|
XP_016885091.1:p.Met2419Leu
|
|
XM_017029603.1:c.7207A>C
|
XP_016885092.1:p.Met2403Leu
|
|
XM_017029604.2:c.7174A>C
|
XP_016885093.1:p.Met2392Leu
|
|
XM_017029605.1:c.7171A>C
|
XP_016885094.1:p.Met2391Leu
|
|
XM_017029606.2:c.7144A>C
|
XP_016885095.1:p.Met2382Leu
|
|
XM_017029607.2:c.7141A>C
|
XP_016885096.1:p.Met2381Leu
|
|
XM_017029608.2:c.7093A>C
|
XP_016885097.1:p.Met2365Leu
|
|
XM_017029609.1:c.7057A>C
|
XP_016885098.1:p.Met2353Leu
|
|
XM_017029610.1:c.7054A>C
|
XP_016885099.1:p.Met2352Leu
|
|
XM_017029611.1:c.7009A>C
|
XP_016885100.1:p.Met2337Leu
|
|
XR_001755700.2:n.7674A>C
|
|
|
NM_138270.4:c.7261A>C
|
NP_612114.2:p.Met2421Leu
|
|
NM_000489.6:c.7375A>C
MANE Select
|
NP_000480.3:p.Met2459Leu
|
|
NM_138270.5:c.7261A>C
|
NP_612114.2:p.Met2421Leu
|
|