ENST00000403733.8:c.3260T>A
MANE Select
|
ENSP00000384222.3:p.Leu1087Gln
|
|
ENST00000403733.7:c.3260T>A
|
ENSP00000384222.3:p.Leu1087Gln
|
|
ENST00000427431.5:c.*2652T>A
|
ENSP00000393342.1:n.*2652T>A
|
|
ENST00000438543.5:c.*1056T>A
|
ENSP00000413521.1:n.*1056T>A
|
|
ENST00000448232.6:c.3332T>A
|
ENSP00000398577.2:p.Leu1111Gln
|
|
ENST00000504005.5:c.2306T>A
|
ENSP00000427569.1:p.Leu769Gln
|
|
ENST00000508747.1:c.644T>A
|
ENSP00000420835.1:p.Leu215Gln
|
|
ENST00000513834.5:c.3113T>A
|
ENSP00000425054.1:p.Leu1038Gln
|
|
NM_024949.5:c.3260T>A
|
NP_079225.5:p.Leu1087Gln
|
|
XM_011532269.1:c.3332T>A
|
XP_011530571.1:p.Leu1111Gln
|
|
XM_011532269.3:c.3332T>A
|
XP_011530571.1:p.Leu1111Gln
|
|
XM_024454225.1:c.3038T>A
|
XP_024309993.1:p.Leu1013Gln
|
|
NM_024949.6:c.3260T>A
MANE Select
|
NP_079225.5:p.Leu1087Gln
|
|