ENST00000373344.11:c.7090C>A
MANE Select
|
ENSP00000362441.4:p.Leu2364Ile
|
|
ENST00000675732.1:c.2188C>A
|
ENSP00000502598.1:p.Leu730Ile
|
|
ENST00000373344.9:c.7090C>A
|
ENSP00000362441.4:p.Leu2364Ile
|
|
ENST00000395603.7:c.6976C>A
|
ENSP00000378967.3:p.Leu2326Ile
|
|
ENST00000480283.5:c.*6718C>A
|
ENSP00000480196.1:n.*6718C>A
|
|
ENST00000623706.3:n.5410C>A
|
|
|
ENST00000624766.1:n.321C>A
|
|
|
NM_000489.4:c.7090C>A
|
NP_000480.3:p.Leu2364Ile
|
|
NM_138270.3:c.6976C>A
|
NP_612114.2:p.Leu2326Ile
|
|
XM_005262153.3:c.7087C>A
|
XP_005262210.2:p.Leu2363Ile
|
|
XM_005262154.3:c.7003C>A
|
XP_005262211.2:p.Leu2335Ile
|
|
XM_005262155.3:c.6973C>A
|
XP_005262212.2:p.Leu2325Ile
|
|
XM_005262156.3:c.6925C>A
|
XP_005262213.2:p.Leu2309Ile
|
|
XM_005262157.3:c.6886C>A
|
XP_005262214.2:p.Leu2296Ile
|
|
XM_006724666.2:c.6973C>A
|
XP_006724729.1:p.Leu2325Ile
|
|
XM_006724667.2:c.6811C>A
|
XP_006724730.1:p.Leu2271Ile
|
|
XR_938400.1:n.8682C>A
|
|
|
NM_000489.5:c.7090C>A
|
NP_000480.3:p.Leu2364Ile
|
|
XM_005262153.5:c.7087C>A
|
XP_005262210.2:p.Leu2363Ile
|
|
XM_005262154.5:c.7003C>A
|
XP_005262211.2:p.Leu2335Ile
|
|
XM_005262155.4:c.6973C>A
|
XP_005262212.2:p.Leu2325Ile
|
|
XM_005262156.4:c.6925C>A
|
XP_005262213.2:p.Leu2309Ile
|
|
XM_005262157.5:c.6886C>A
|
XP_005262214.2:p.Leu2296Ile
|
|
XM_006724666.4:c.6973C>A
|
XP_006724729.1:p.Leu2325Ile
|
|
XM_006724667.3:c.6811C>A
|
XP_006724730.1:p.Leu2271Ile
|
|
XM_017029601.2:c.7000C>A
|
XP_016885090.1:p.Leu2334Ile
|
|
XM_017029602.1:c.6970C>A
|
XP_016885091.1:p.Leu2324Ile
|
|
XM_017029603.1:c.6922C>A
|
XP_016885092.1:p.Leu2308Ile
|
|
XM_017029604.2:c.6889C>A
|
XP_016885093.1:p.Leu2297Ile
|
|
XM_017029605.1:c.6886C>A
|
XP_016885094.1:p.Leu2296Ile
|
|
XM_017029606.2:c.6859C>A
|
XP_016885095.1:p.Leu2287Ile
|
|
XM_017029607.2:c.6856C>A
|
XP_016885096.1:p.Leu2286Ile
|
|
XM_017029608.2:c.6808C>A
|
XP_016885097.1:p.Leu2270Ile
|
|
XM_017029609.1:c.6772C>A
|
XP_016885098.1:p.Leu2258Ile
|
|
XM_017029610.1:c.6769C>A
|
XP_016885099.1:p.Leu2257Ile
|
|
XM_017029611.1:c.6724C>A
|
XP_016885100.1:p.Leu2242Ile
|
|
XR_001755700.2:n.7389C>A
|
|
|
NM_138270.4:c.6976C>A
|
NP_612114.2:p.Leu2326Ile
|
|
NM_000489.6:c.7090C>A
MANE Select
|
NP_000480.3:p.Leu2364Ile
|
|
NM_138270.5:c.6976C>A
|
NP_612114.2:p.Leu2326Ile
|
|