ENST00000373344.11:c.7436T>C
MANE Select
|
ENSP00000362441.4:p.Met2479Thr
|
|
ENST00000675732.1:c.2534T>C
|
ENSP00000502598.1:p.Met845Thr
|
|
ENST00000373344.9:c.7436T>C
|
ENSP00000362441.4:p.Met2479Thr
|
|
ENST00000395603.7:c.7322T>C
|
ENSP00000378967.3:p.Met2441Thr
|
|
ENST00000480283.5:c.*7064T>C
|
ENSP00000480196.1:n.*7064T>C
|
|
ENST00000623706.3:n.5756T>C
|
|
|
NM_000489.4:c.7436T>C
|
NP_000480.3:p.Met2479Thr
|
|
NM_138270.3:c.7322T>C
|
NP_612114.2:p.Met2441Thr
|
|
XM_005262153.3:c.7433T>C
|
XP_005262210.2:p.Met2478Thr
|
|
XM_005262154.3:c.7349T>C
|
XP_005262211.2:p.Met2450Thr
|
|
XM_005262155.3:c.7319T>C
|
XP_005262212.2:p.Met2440Thr
|
|
XM_005262156.3:c.7271T>C
|
XP_005262213.2:p.Met2424Thr
|
|
XM_005262157.3:c.7232T>C
|
XP_005262214.2:p.Met2411Thr
|
|
XM_006724666.2:c.7319T>C
|
XP_006724729.1:p.Met2440Thr
|
|
XM_006724667.2:c.7157T>C
|
XP_006724730.1:p.Met2386Thr
|
|
XR_938400.1:n.9028T>C
|
|
|
NM_000489.5:c.7436T>C
|
NP_000480.3:p.Met2479Thr
|
|
XM_005262153.5:c.7433T>C
|
XP_005262210.2:p.Met2478Thr
|
|
XM_005262154.5:c.7349T>C
|
XP_005262211.2:p.Met2450Thr
|
|
XM_005262155.4:c.7319T>C
|
XP_005262212.2:p.Met2440Thr
|
|
XM_005262156.4:c.7271T>C
|
XP_005262213.2:p.Met2424Thr
|
|
XM_005262157.5:c.7232T>C
|
XP_005262214.2:p.Met2411Thr
|
|
XM_006724666.4:c.7319T>C
|
XP_006724729.1:p.Met2440Thr
|
|
XM_006724667.3:c.7157T>C
|
XP_006724730.1:p.Met2386Thr
|
|
XM_017029601.2:c.7346T>C
|
XP_016885090.1:p.Met2449Thr
|
|
XM_017029602.1:c.7316T>C
|
XP_016885091.1:p.Met2439Thr
|
|
XM_017029603.1:c.7268T>C
|
XP_016885092.1:p.Met2423Thr
|
|
XM_017029604.2:c.7235T>C
|
XP_016885093.1:p.Met2412Thr
|
|
XM_017029605.1:c.7232T>C
|
XP_016885094.1:p.Met2411Thr
|
|
XM_017029606.2:c.7205T>C
|
XP_016885095.1:p.Met2402Thr
|
|
XM_017029607.2:c.7202T>C
|
XP_016885096.1:p.Met2401Thr
|
|
XM_017029608.2:c.7154T>C
|
XP_016885097.1:p.Met2385Thr
|
|
XM_017029609.1:c.7118T>C
|
XP_016885098.1:p.Met2373Thr
|
|
XM_017029610.1:c.7115T>C
|
XP_016885099.1:p.Met2372Thr
|
|
XM_017029611.1:c.7070T>C
|
XP_016885100.1:p.Met2357Thr
|
|
XR_001755700.2:n.7735T>C
|
|
|
NM_138270.4:c.7322T>C
|
NP_612114.2:p.Met2441Thr
|
|
NM_000489.6:c.7436T>C
MANE Select
|
NP_000480.3:p.Met2479Thr
|
|
NM_138270.5:c.7322T>C
|
NP_612114.2:p.Met2441Thr
|
|