ENST00000373344.11:c.7435A>T
MANE Select
|
ENSP00000362441.4:p.Met2479Leu
|
|
ENST00000675732.1:c.2533A>T
|
ENSP00000502598.1:p.Met845Leu
|
|
ENST00000373344.9:c.7435A>T
|
ENSP00000362441.4:p.Met2479Leu
|
|
ENST00000395603.7:c.7321A>T
|
ENSP00000378967.3:p.Met2441Leu
|
|
ENST00000480283.5:c.*7063A>T
|
ENSP00000480196.1:n.*7063A>T
|
|
ENST00000623706.3:n.5755A>T
|
|
|
NM_000489.4:c.7435A>T
|
NP_000480.3:p.Met2479Leu
|
|
NM_138270.3:c.7321A>T
|
NP_612114.2:p.Met2441Leu
|
|
XM_005262153.3:c.7432A>T
|
XP_005262210.2:p.Met2478Leu
|
|
XM_005262154.3:c.7348A>T
|
XP_005262211.2:p.Met2450Leu
|
|
XM_005262155.3:c.7318A>T
|
XP_005262212.2:p.Met2440Leu
|
|
XM_005262156.3:c.7270A>T
|
XP_005262213.2:p.Met2424Leu
|
|
XM_005262157.3:c.7231A>T
|
XP_005262214.2:p.Met2411Leu
|
|
XM_006724666.2:c.7318A>T
|
XP_006724729.1:p.Met2440Leu
|
|
XM_006724667.2:c.7156A>T
|
XP_006724730.1:p.Met2386Leu
|
|
XR_938400.1:n.9027A>T
|
|
|
NM_000489.5:c.7435A>T
|
NP_000480.3:p.Met2479Leu
|
|
XM_005262153.5:c.7432A>T
|
XP_005262210.2:p.Met2478Leu
|
|
XM_005262154.5:c.7348A>T
|
XP_005262211.2:p.Met2450Leu
|
|
XM_005262155.4:c.7318A>T
|
XP_005262212.2:p.Met2440Leu
|
|
XM_005262156.4:c.7270A>T
|
XP_005262213.2:p.Met2424Leu
|
|
XM_005262157.5:c.7231A>T
|
XP_005262214.2:p.Met2411Leu
|
|
XM_006724666.4:c.7318A>T
|
XP_006724729.1:p.Met2440Leu
|
|
XM_006724667.3:c.7156A>T
|
XP_006724730.1:p.Met2386Leu
|
|
XM_017029601.2:c.7345A>T
|
XP_016885090.1:p.Met2449Leu
|
|
XM_017029602.1:c.7315A>T
|
XP_016885091.1:p.Met2439Leu
|
|
XM_017029603.1:c.7267A>T
|
XP_016885092.1:p.Met2423Leu
|
|
XM_017029604.2:c.7234A>T
|
XP_016885093.1:p.Met2412Leu
|
|
XM_017029605.1:c.7231A>T
|
XP_016885094.1:p.Met2411Leu
|
|
XM_017029606.2:c.7204A>T
|
XP_016885095.1:p.Met2402Leu
|
|
XM_017029607.2:c.7201A>T
|
XP_016885096.1:p.Met2401Leu
|
|
XM_017029608.2:c.7153A>T
|
XP_016885097.1:p.Met2385Leu
|
|
XM_017029609.1:c.7117A>T
|
XP_016885098.1:p.Met2373Leu
|
|
XM_017029610.1:c.7114A>T
|
XP_016885099.1:p.Met2372Leu
|
|
XM_017029611.1:c.7069A>T
|
XP_016885100.1:p.Met2357Leu
|
|
XR_001755700.2:n.7734A>T
|
|
|
NM_138270.4:c.7321A>T
|
NP_612114.2:p.Met2441Leu
|
|
NM_000489.6:c.7435A>T
MANE Select
|
NP_000480.3:p.Met2479Leu
|
|
NM_138270.5:c.7321A>T
|
NP_612114.2:p.Met2441Leu
|
|