ENST00000373344.11:c.7409C>T
MANE Select
|
ENSP00000362441.4:p.Pro2470Leu
|
|
ENST00000675732.1:c.2507C>T
|
ENSP00000502598.1:p.Pro836Leu
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|
ENST00000373344.9:c.7409C>T
|
ENSP00000362441.4:p.Pro2470Leu
|
|
ENST00000395603.7:c.7295C>T
|
ENSP00000378967.3:p.Pro2432Leu
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|
ENST00000480283.5:c.*7037C>T
|
ENSP00000480196.1:n.*7037C>T
|
|
ENST00000623706.3:n.5729C>T
|
|
|
NM_000489.4:c.7409C>T
|
NP_000480.3:p.Pro2470Leu
|
|
NM_138270.3:c.7295C>T
|
NP_612114.2:p.Pro2432Leu
|
|
XM_005262153.3:c.7406C>T
|
XP_005262210.2:p.Pro2469Leu
|
|
XM_005262154.3:c.7322C>T
|
XP_005262211.2:p.Pro2441Leu
|
|
XM_005262155.3:c.7292C>T
|
XP_005262212.2:p.Pro2431Leu
|
|
XM_005262156.3:c.7244C>T
|
XP_005262213.2:p.Pro2415Leu
|
|
XM_005262157.3:c.7205C>T
|
XP_005262214.2:p.Pro2402Leu
|
|
XM_006724666.2:c.7292C>T
|
XP_006724729.1:p.Pro2431Leu
|
|
XM_006724667.2:c.7130C>T
|
XP_006724730.1:p.Pro2377Leu
|
|
XR_938400.1:n.9001C>T
|
|
|
NM_000489.5:c.7409C>T
|
NP_000480.3:p.Pro2470Leu
|
|
XM_005262153.5:c.7406C>T
|
XP_005262210.2:p.Pro2469Leu
|
|
XM_005262154.5:c.7322C>T
|
XP_005262211.2:p.Pro2441Leu
|
|
XM_005262155.4:c.7292C>T
|
XP_005262212.2:p.Pro2431Leu
|
|
XM_005262156.4:c.7244C>T
|
XP_005262213.2:p.Pro2415Leu
|
|
XM_005262157.5:c.7205C>T
|
XP_005262214.2:p.Pro2402Leu
|
|
XM_006724666.4:c.7292C>T
|
XP_006724729.1:p.Pro2431Leu
|
|
XM_006724667.3:c.7130C>T
|
XP_006724730.1:p.Pro2377Leu
|
|
XM_017029601.2:c.7319C>T
|
XP_016885090.1:p.Pro2440Leu
|
|
XM_017029602.1:c.7289C>T
|
XP_016885091.1:p.Pro2430Leu
|
|
XM_017029603.1:c.7241C>T
|
XP_016885092.1:p.Pro2414Leu
|
|
XM_017029604.2:c.7208C>T
|
XP_016885093.1:p.Pro2403Leu
|
|
XM_017029605.1:c.7205C>T
|
XP_016885094.1:p.Pro2402Leu
|
|
XM_017029606.2:c.7178C>T
|
XP_016885095.1:p.Pro2393Leu
|
|
XM_017029607.2:c.7175C>T
|
XP_016885096.1:p.Pro2392Leu
|
|
XM_017029608.2:c.7127C>T
|
XP_016885097.1:p.Pro2376Leu
|
|
XM_017029609.1:c.7091C>T
|
XP_016885098.1:p.Pro2364Leu
|
|
XM_017029610.1:c.7088C>T
|
XP_016885099.1:p.Pro2363Leu
|
|
XM_017029611.1:c.7043C>T
|
XP_016885100.1:p.Pro2348Leu
|
|
XR_001755700.2:n.7708C>T
|
|
|
NM_138270.4:c.7295C>T
|
NP_612114.2:p.Pro2432Leu
|
|
NM_000489.6:c.7409C>T
MANE Select
|
NP_000480.3:p.Pro2470Leu
|
|
NM_138270.5:c.7295C>T
|
NP_612114.2:p.Pro2432Leu
|
|