ENST00000391944.8:c.2136G>T
|
ENSP00000375808.4:p.Glu712Asp
|
|
ENST00000682414.1:c.2136G>T
|
ENSP00000507019.1:p.Glu712Asp
|
|
ENST00000682508.1:n.2165G>T
|
|
|
ENST00000684218.1:c.*1394G>T
|
ENSP00000507804.1:n.*1394G>T
|
|
ENST00000684264.1:n.1692G>T
|
|
|
ENST00000684407.1:c.2013G>T
|
ENSP00000507775.1:p.Glu671Asp
|
|
ENST00000684458.1:c.*622G>T
|
ENSP00000508260.1:n.*622G>T
|
|
ENST00000684468.1:n.1848G>T
|
|
|
ENST00000391945.10:c.2136G>T
MANE Select
|
ENSP00000375809.4:p.Glu712Asp
|
|
ENST00000646507.1:n.2233G>T
|
|
|
ENST00000391941.6:c.2064G>T
|
ENSP00000375805.2:p.Glu688Asp
|
|
ENST00000391942.6:n.1307G>T
|
|
|
ENST00000391944.7:c.1902G>T
|
ENSP00000375808.3:p.Glu634Asp
|
|
ENST00000391945.8:c.2136G>T
|
ENSP00000375809.3:p.Glu712Asp
|
|
ENST00000588652.5:n.2224G>T
|
|
|
NM_000400.3:c.2136G>T , LRG_461t1:c.2136G>T
|
NP_000391.1:p.Glu712Asp
|
|
XM_011526611.1:c.2058G>T
|
XP_011524913.1:p.Glu686Asp
|
|
XM_011526611.2:c.2058G>T
|
XP_011524913.1:p.Glu686Asp
|
|
XM_017026467.1:c.2013G>T
|
XP_016881956.1:p.Glu671Asp
|
|
XR_001753633.2:n.2183G>T
|
|
|
XR_001753634.2:n.2119G>T
|
|
|
NM_000400.4:c.2136G>T
MANE Select
|
NP_000391.1:p.Glu712Asp
|
|