ENST00000403733.8:c.3175C>T
MANE Select
|
ENSP00000384222.3:p.Gln1059Ter
|
|
ENST00000403733.7:c.3175C>T
|
ENSP00000384222.3:p.Gln1059Ter
|
|
ENST00000427431.5:c.*2567C>T
|
ENSP00000393342.1:n.*2567C>T
|
|
ENST00000438543.5:c.*971C>T
|
ENSP00000413521.1:n.*971C>T
|
|
ENST00000448232.6:c.3247C>T
|
ENSP00000398577.2:p.Gln1083Ter
|
|
ENST00000504005.5:c.2221C>T
|
ENSP00000427569.1:p.Gln741Ter
|
|
ENST00000508747.1:c.559C>T
|
ENSP00000420835.1:p.Gln187Ter
|
|
ENST00000513834.5:c.3028C>T
|
ENSP00000425054.1:p.Gln1010Ter
|
|
NM_024949.5:c.3175C>T
|
NP_079225.5:p.Gln1059Ter
|
|
XM_011532269.1:c.3247C>T
|
XP_011530571.1:p.Gln1083Ter
|
|
XM_011532269.3:c.3247C>T
|
XP_011530571.1:p.Gln1083Ter
|
|
XM_024454225.1:c.2953C>T
|
XP_024309993.1:p.Gln985Ter
|
|
NM_024949.6:c.3175C>T
MANE Select
|
NP_079225.5:p.Gln1059Ter
|
|