ENST00000409709.9:c.6121A>T
MANE Select
|
ENSP00000386331.3:p.Ile2041Phe
|
|
ENST00000670577.1:c.3922A>T
|
|
|
ENST00000409619.6:c.5974A>T
|
ENSP00000386635.2:p.Ile1992Phe
|
|
ENST00000409709.7:c.6121A>T
|
ENSP00000386331.3:p.Ile2041Phe
|
|
ENST00000458169.2:c.3547A>T
|
ENSP00000417017.2:p.Ile1183Phe
|
|
ENST00000458637.6:c.6007A>T
|
ENSP00000392185.2:p.Ile2003Phe
|
|
ENST00000481328.7:n.3657A>T
|
|
|
ENST00000526863.2:n.25+310A>T
|
|
|
ENST00000605744.1:n.1588A>T
|
|
|
NM_000260.3:c.6121A>T
|
NP_000251.3:p.Ile2041Phe
|
|
NM_001127180.1:c.6007A>T
|
NP_001120652.1:p.Ile2003Phe
|
|
XM_005274012.2:c.6004A>T
|
XP_005274069.1:p.Ile2002Phe
|
|
XM_006718558.2:c.6112A>T
|
XP_006718621.1:p.Ile2038Phe
|
|
XM_006718559.2:c.6007A>T
|
XP_006718622.1:p.Ile2003Phe
|
|
XM_006718560.2:c.6004A>T
|
XP_006718623.1:p.Ile2002Phe
|
|
XM_006718561.2:c.6007A>T
|
XP_006718624.1:p.Ile2003Phe
|
|
XM_011545044.1:c.6121A>T
|
XP_011543346.1:p.Ile2041Phe
|
|
XM_011545045.1:c.6115A>T
|
XP_011543347.1:p.Ile2039Phe
|
|
XM_011545046.1:c.6088A>T
|
XP_011543348.1:p.Ile2030Phe
|
|
XM_011545047.1:c.6025A>T
|
XP_011543349.1:p.Ile2009Phe
|
|
XM_011545048.1:c.5896A>T
|
XP_011543350.1:p.Ile1966Phe
|
|
XM_011545049.1:c.5884A>T
|
XP_011543351.1:p.Ile1962Phe
|
|
XM_011545050.1:c.5857A>T
|
XP_011543352.1:p.Ile1953Phe
|
|
XM_011545051.1:c.6121A>T
|
XP_011543353.1:p.Ile2041Phe
|
|
XR_949938.1:n.6441A>T
|
|
|
XR_949941.1:n.6415A>T
|
|
|
XM_011545044.2:c.6121A>T
|
XP_011543346.1:p.Ile2041Phe
|
|
XM_011545046.2:c.6211A>T
|
XP_011543348.2:p.Ile2071Phe
|
|
XM_011545050.2:c.5857A>T
|
XP_011543352.1:p.Ile1953Phe
|
|
XM_017017778.1:c.6205A>T
|
XP_016873267.1:p.Ile2069Phe
|
|
XM_017017779.1:c.6202A>T
|
XP_016873268.1:p.Ile2068Phe
|
|
XM_017017780.1:c.6211A>T
|
XP_016873269.1:p.Ile2071Phe
|
|
XM_017017781.1:c.6115A>T
|
XP_016873270.1:p.Ile2039Phe
|
|
XM_017017782.1:c.6097A>T
|
XP_016873271.1:p.Ile2033Phe
|
|
XM_017017783.1:c.6094A>T
|
XP_016873272.1:p.Ile2032Phe
|
|
XM_017017784.1:c.6094A>T
|
XP_016873273.1:p.Ile2032Phe
|
|
XM_017017785.1:c.5974A>T
|
XP_016873274.1:p.Ile1992Phe
|
|
XM_017017786.1:c.6211A>T
|
XP_016873275.1:p.Ile2071Phe
|
|
XM_017017788.1:c.6097A>T
|
XP_016873277.1:p.Ile2033Phe
|
|
XR_001747885.1:n.6200A>T
|
|
|
XR_001747886.1:n.6141A>T
|
|
|
XR_001747887.1:n.6186A>T
|
|
|
NM_000260.4:c.6121A>T
MANE Select
|
NP_000251.3:p.Ile2041Phe
|
|
NM_001127180.2:c.6007A>T
|
NP_001120652.1:p.Ile2003Phe
|
|
NM_001369365.1:c.5974A>T
|
NP_001356294.1:p.Ile1992Phe
|
|