ENST00000600737.6:c.2772G>C
MANE Select
|
ENSP00000473211.1:p.Leu924=
|
|
ENST00000221249.10:c.2658G>C
|
ENSP00000221249.5:p.Leu886=
|
|
ENST00000414982.7:c.2802G>C
|
ENSP00000407509.2:p.Leu934=
|
|
ENST00000450331.7:c.2658G>C
|
ENSP00000394348.2:p.Leu886=
|
|
ENST00000545201.6:c.2577G>C
|
ENSP00000443323.1:p.Leu859=
|
|
ENST00000600737.5:c.2772G>C
|
ENSP00000473211.1:p.Leu924=
|
|
NM_001166111.1:c.2802G>C
|
NP_001159583.1:p.Leu934=
|
|
NM_001166112.1:c.2577G>C
|
NP_001159584.1:p.Leu859=
|
|
NM_001166113.1:c.2658G>C
|
NP_001159585.1:p.Leu886=
|
|
NM_001166114.1:c.2772G>C
|
NP_001159586.1:p.Leu924=
|
|
NM_006702.4:c.2658G>C
|
NP_006693.3:p.Leu886=
|
|
NM_001166111.2:c.2802G>C
|
NP_001159583.1:p.Leu934=
|
|
NM_001166114.2:c.2772G>C
MANE Select
|
NP_001159586.1:p.Leu924=
|
|
NM_006702.5:c.2658G>C
|
NP_006693.3:p.Leu886=
|
|
NM_001166112.2:c.2577G>C
|
NP_001159584.1:p.Leu859=
|
|