ENST00000698057.1:c.3030G>A
|
ENSP00000513536.1:p.Glu1010=
|
|
ENST00000698058.1:c.2247G>A
|
ENSP00000513537.1:p.Glu749=
|
|
ENST00000698059.1:c.2355G>A
|
ENSP00000513538.1:p.Glu785=
|
|
ENST00000258104.8:c.5499G>A
MANE Plus Clinical
|
ENSP00000258104.3:p.Glu1833=
|
|
ENST00000410020.8:c.5616G>A
MANE Select
|
ENSP00000386881.3:p.Glu1872=
|
|
ENST00000258104.7:c.5499G>A
|
ENSP00000258104.3:p.Glu1833=
|
|
ENST00000394120.6:c.5502G>A
|
ENSP00000377678.2:p.Glu1834=
|
|
ENST00000409366.5:c.5565G>A
|
ENSP00000386512.1:p.Glu1855=
|
|
ENST00000409582.7:c.5613G>A
|
ENSP00000386547.3:p.Glu1871=
|
|
ENST00000409651.5:c.5595G>A
|
ENSP00000386683.1:p.Glu1865=
|
|
ENST00000409744.5:c.5523G>A
|
ENSP00000386285.1:p.Glu1841=
|
|
ENST00000409762.5:c.5550G>A
|
ENSP00000387137.1:p.Glu1850=
|
|
ENST00000410020.7:c.5616G>A
|
ENSP00000386881.3:p.Glu1872=
|
|
ENST00000410041.1:c.5553G>A
|
ENSP00000386617.1:p.Glu1851=
|
|
ENST00000413539.6:c.5592G>A
|
ENSP00000407046.2:p.Glu1864=
|
|
ENST00000429174.6:c.5562G>A
|
ENSP00000398305.2:p.Glu1854=
|
|
ENST00000479049.6:n.2384G>A
|
|
|
NM_001130455.1:c.5502G>A
|
NP_001123927.1:p.Glu1834=
|
|
NM_001130976.1:c.5457G>A
|
NP_001124448.1:p.Glu1819=
|
|
NM_001130977.1:c.5520G>A
|
NP_001124449.1:p.Glu1840=
|
|
NM_001130978.1:c.5562G>A
|
NP_001124450.1:p.Glu1854=
|
|
NM_001130979.1:c.5592G>A
|
NP_001124451.1:p.Glu1864=
|
|
NM_001130980.1:c.5550G>A
|
NP_001124452.1:p.Glu1850=
|
|
NM_001130981.1:c.5613G>A
|
NP_001124453.1:p.Glu1871=
|
|
NM_001130982.1:c.5595G>A
|
NP_001124454.1:p.Glu1865=
|
|
NM_001130983.1:c.5565G>A
|
NP_001124455.1:p.Glu1855=
|
|
NM_001130984.1:c.5523G>A
|
NP_001124456.1:p.Glu1841=
|
|
NM_001130985.1:c.5553G>A
|
NP_001124457.1:p.Glu1851=
|
|
NM_001130986.1:c.5460G>A
|
NP_001124458.1:p.Glu1820=
|
|
NM_001130987.1:c.5616G>A
|
NP_001124459.1:p.Glu1872=
|
|
NM_003494.3:c.5499G>A
|
NP_003485.1:p.Glu1833=
|
|
XM_005264584.3:c.5658G>A
|
XP_005264641.1:p.Glu1886=
|
|
XM_005264585.3:c.5655G>A
|
XP_005264642.1:p.Glu1885=
|
|
XM_005264584.4:c.5658G>A
|
XP_005264641.1:p.Glu1886=
|
|
XM_005264585.5:c.5655G>A
|
XP_005264642.1:p.Glu1885=
|
|
NM_001130987.2:c.5616G>A
MANE Select
|
NP_001124459.1:p.Glu1872=
|
|
NM_001130455.2:c.5502G>A
|
NP_001123927.1:p.Glu1834=
|
|
NM_001130976.2:c.5457G>A
|
NP_001124448.1:p.Glu1819=
|
|
NM_001130977.2:c.5520G>A
|
NP_001124449.1:p.Glu1840=
|
|
NM_001130978.2:c.5562G>A
|
NP_001124450.1:p.Glu1854=
|
|
NM_001130979.2:c.5592G>A
|
NP_001124451.1:p.Glu1864=
|
|
NM_001130980.2:c.5550G>A
|
NP_001124452.1:p.Glu1850=
|
|
NM_001130981.2:c.5613G>A
|
NP_001124453.1:p.Glu1871=
|
|
NM_001130982.2:c.5595G>A
|
NP_001124454.1:p.Glu1865=
|
|
NM_001130983.2:c.5565G>A
|
NP_001124455.1:p.Glu1855=
|
|
NM_001130984.2:c.5523G>A
|
NP_001124456.1:p.Glu1841=
|
|
NM_001130985.2:c.5553G>A
|
NP_001124457.1:p.Glu1851=
|
|
NM_001130986.2:c.5460G>A
|
NP_001124458.1:p.Glu1820=
|
|
NM_003494.4:c.5499G>A
MANE Plus Clinical
|
NP_003485.1:p.Glu1833=
|
|