ENST00000355832.10:c.3709G>T
MANE Select
|
ENSP00000348089.5:p.Glu1237Ter
|
|
ENST00000679552.1:n.780G>T
|
|
|
ENST00000679871.1:n.855G>T
|
|
|
ENST00000679974.1:n.758G>T
|
|
|
ENST00000681632.1:n.5112G>T
|
|
|
ENST00000681659.1:c.3550G>T
|
ENSP00000505631.1:p.Glu1184Ter
|
|
ENST00000355832.9:c.3709G>T
|
ENSP00000348089.5:p.Glu1237Ter
|
|
ENST00000465653.1:n.31G>T
|
|
|
ENST00000623073.3:c.*2005G>T
|
ENSP00000485650.1:n.*2005G>T
|
|
ENST00000623115.3:c.1819G>T
|
ENSP00000485321.1:p.Glu607Ter
|
|
ENST00000624341.3:c.1541G>T
|
|
|
NM_000124.3:c.3709G>T
|
NP_000115.1:p.Glu1237Ter
|
|
XR_945953.1:n.243-1314C>A
|
|
|
NM_001346440.1:c.3709G>T
|
NP_001333369.1:p.Glu1237Ter
|
|
NM_000124.4:c.3709G>T
MANE Select
|
NP_000115.1:p.Glu1237Ter
|
|
NM_001346440.2:c.3709G>T
|
NP_001333369.1:p.Glu1237Ter
|
|