ENST00000371757.7:c.2302C>G
MANE Select
|
ENSP00000360822.2:p.His768Asp
|
|
ENST00000674572.1:c.2143C>G
|
ENSP00000501742.1:p.His715Asp
|
|
ENST00000675090.1:c.2050C>G
|
ENSP00000501833.1:p.His684Asp
|
|
ENST00000675399.1:c.2050C>G
|
ENSP00000501932.1:p.His684Asp
|
|
ENST00000676421.1:c.2059C>G
|
ENSP00000502322.1:p.His687Asp
|
|
ENST00000263604.5:c.2203C>G
|
ENSP00000263604.4:p.His735Asp
|
|
ENST00000371757.6:c.2302C>G
|
ENSP00000360822.2:p.His768Asp
|
|
ENST00000460750.5:c.*1912C>G
|
ENSP00000418777.1:n.*1912C>G
|
|
ENST00000486577.6:c.2185C>G
|
ENSP00000417578.3:p.His729Asp
|
|
ENST00000487664.5:c.2302C>G
|
ENSP00000417851.2:p.His768Asp
|
|
ENST00000488444.6:c.2245C>G
|
ENSP00000419007.3:p.His749Asp
|
|
ENST00000490355.6:c.2239C>G
|
ENSP00000418003.3:p.His747Asp
|
|
ENST00000490363.3:n.2121C>G
|
|
|
ENST00000491806.6:c.2245C>G
|
ENSP00000419086.3:p.His749Asp
|
|
ENST00000628528.2:c.2167C>G
|
ENSP00000486374.1:p.His723Asp
|
|
ENST00000630792.2:c.2137C>G
|
ENSP00000486486.1:p.His713Asp
|
|
ENST00000631073.2:c.2245C>G
|
ENSP00000486130.1:p.His749Asp
|
|
ENST00000631193.1:c.151C>G
|
ENSP00000486830.1:p.His51Asp
|
|
NM_001272003.1:c.2167C>G
|
NP_001258932.1:p.His723Asp
|
|
NM_020822.2:c.2302C>G
|
NP_065873.2:p.His768Asp
|
|
XM_011518877.1:c.2437C>G
|
XP_011517179.1:p.His813Asp
|
|
XM_011518878.1:c.2446C>G
|
XP_011517180.1:p.His816Asp
|
|
XM_011518879.1:c.2437C>G
|
XP_011517181.1:p.His813Asp
|
|
XM_011518880.1:c.2203C>G
|
XP_011517182.1:p.His735Asp
|
|
XM_011518881.1:c.1792C>G
|
XP_011517183.1:p.His598Asp
|
|
XM_011518877.3:c.2437C>G
|
XP_011517179.1:p.His813Asp
|
|
XM_011518878.3:c.2446C>G
|
XP_011517180.1:p.His816Asp
|
|
XM_011518879.3:c.2437C>G
|
XP_011517181.1:p.His813Asp
|
|
XM_011518881.3:c.1792C>G
|
XP_011517183.1:p.His598Asp
|
|
XM_017014931.1:c.2236C>G
|
XP_016870420.1:p.His746Asp
|
|
XM_017014932.1:c.2059C>G
|
XP_016870421.1:p.His687Asp
|
|
XM_017014933.1:c.1792C>G
|
XP_016870422.1:p.His598Asp
|
|
XM_024447617.1:c.1792C>G
|
XP_024303385.1:p.His598Asp
|
|
XM_024447618.1:c.1792C>G
|
XP_024303386.1:p.His598Asp
|
|
NM_020822.3:c.2302C>G
MANE Select
|
NP_065873.2:p.His768Asp
|
|
NM_001272003.2:c.2167C>G
|
NP_001258932.1:p.His723Asp
|
|