|
NM_001130987.2:c.3805C>T
MANE Select
|
NP_001124459.1:p.Arg1269Trp
|
|
ENST00000410020.8:c.3805C>T
MANE Select
|
ENSP00000386881.3:p.Arg1269Trp
|
|
NM_003494.4:c.3751C>T
MANE Plus Clinical
|
NP_003485.1:p.Arg1251Trp
|
|
ENST00000258104.8:c.3751C>T
MANE Plus Clinical
|
ENSP00000258104.3:p.Arg1251Trp
|
|
NM_001130455.1:c.3754C>T
|
NP_001123927.1:p.Arg1252Trp
|
|
NM_001130455.2:c.3754C>T
|
NP_001123927.1:p.Arg1252Trp
|
|
NM_001130976.1:c.3709C>T
|
NP_001124448.1:p.Arg1237Trp
|
|
NM_001130976.2:c.3709C>T
|
NP_001124448.1:p.Arg1237Trp
|
|
NM_001130977.1:c.3709C>T
|
NP_001124449.1:p.Arg1237Trp
|
|
NM_001130977.2:c.3709C>T
|
NP_001124449.1:p.Arg1237Trp
|
|
NM_001130978.1:c.3751C>T
|
NP_001124450.1:p.Arg1251Trp
|
|
NM_001130978.2:c.3751C>T
|
NP_001124450.1:p.Arg1251Trp
|
|
NM_001130979.1:c.3844C>T
|
NP_001124451.1:p.Arg1282Trp
|
|
NM_001130979.2:c.3844C>T
|
NP_001124451.1:p.Arg1282Trp
|
|
NM_001130980.1:c.3802C>T
|
NP_001124452.1:p.Arg1268Trp
|
|
NM_001130980.2:c.3802C>T
|
NP_001124452.1:p.Arg1268Trp
|
|
NM_001130981.1:c.3802C>T
|
NP_001124453.1:p.Arg1268Trp
|
|
NM_001130981.2:c.3802C>T
|
NP_001124453.1:p.Arg1268Trp
|
|
NM_001130982.1:c.3847C>T
|
NP_001124454.1:p.Arg1283Trp
|
|
NM_001130982.2:c.3847C>T
|
NP_001124454.1:p.Arg1283Trp
|
|
NM_001130983.1:c.3754C>T
|
NP_001124455.1:p.Arg1252Trp
|
|
NM_001130983.2:c.3754C>T
|
NP_001124455.1:p.Arg1252Trp
|
|
NM_001130984.1:c.3712C>T
|
NP_001124456.1:p.Arg1238Trp
|
|
NM_001130984.2:c.3712C>T
|
NP_001124456.1:p.Arg1238Trp
|
|
NM_001130985.1:c.3805C>T
|
NP_001124457.1:p.Arg1269Trp
|
|
NM_001130985.2:c.3805C>T
|
NP_001124457.1:p.Arg1269Trp
|
|
NM_001130986.1:c.3712C>T
|
NP_001124458.1:p.Arg1238Trp
|
|
NM_001130986.2:c.3712C>T
|
NP_001124458.1:p.Arg1238Trp
|
|
NM_001130987.1:c.3805C>T
|
NP_001124459.1:p.Arg1269Trp
|
|
NM_003494.3:c.3751C>T
|
NP_003485.1:p.Arg1251Trp
|
|
ENST00000258104.7:c.3751C>T
|
ENSP00000258104.3:p.Arg1251Trp
|
|
ENST00000394120.6:c.3754C>T
|
ENSP00000377678.2:p.Arg1252Trp
|
|
ENST00000409366.5:c.3754C>T
|
ENSP00000386512.1:p.Arg1252Trp
|
|
ENST00000409582.7:c.3802C>T
|
ENSP00000386547.3:p.Arg1268Trp
|
|
ENST00000409651.5:c.3847C>T
|
ENSP00000386683.1:p.Arg1283Trp
|
|
ENST00000409744.5:c.3712C>T
|
ENSP00000386285.1:p.Arg1238Trp
|
|
ENST00000409762.5:c.3802C>T
|
ENSP00000387137.1:p.Arg1268Trp
|
|
ENST00000410020.7:c.3805C>T
|
ENSP00000386881.3:p.Arg1269Trp
|
|
ENST00000410041.1:c.3805C>T
|
ENSP00000386617.1:p.Arg1269Trp
|
|
ENST00000413539.6:c.3844C>T
|
ENSP00000407046.2:p.Arg1282Trp
|
|
ENST00000429174.6:c.3751C>T
|
ENSP00000398305.2:p.Arg1251Trp
|
|
ENST00000475076.5:n.579C>T
|
|
|
ENST00000479049.6:n.636C>T
|
|
|
ENST00000493767.1:n.472C>T
|
|
|
ENST00000698057.1:c.1177C>T
|
ENSP00000513536.1:p.Arg393Trp
|
|
ENST00000698058.1:c.394C>T
|
ENSP00000513537.1:p.Arg132Trp
|
|
ENST00000698059.1:c.394C>T
|
ENSP00000513538.1:p.Arg132Trp
|
|
XM_005264584.3:c.3847C>T
|
XP_005264641.1:p.Arg1283Trp
|
|
XM_005264584.4:c.3847C>T
|
XP_005264641.1:p.Arg1283Trp
|
|
XM_005264585.3:c.3844C>T
|
XP_005264642.1:p.Arg1282Trp
|
|
XM_005264585.5:c.3844C>T
|
XP_005264642.1:p.Arg1282Trp
|
|
XR_001738969.1:n.4005C>T
|
|
