ENST00000290866.10:c.2556G>T
MANE Select
|
ENSP00000290866.4:p.Leu852=
|
|
ENST00000290863.10:c.834G>T
|
ENSP00000290863.6:p.Leu278=
|
|
ENST00000290866.9:c.2556G>T
|
ENSP00000290866.4:p.Leu852=
|
|
ENST00000413513.7:c.834G>T
|
ENSP00000392247.3:p.Leu278=
|
|
ENST00000428043.5:c.2556G>T
|
ENSP00000397593.2:p.Leu852=
|
|
ENST00000577647.2:c.834G>T
|
ENSP00000464149.1:p.Leu278=
|
|
ENST00000578839.5:c.*519+256G>T
|
ENSP00000462110.2:n.*519+256G>T
|
|
ENST00000579314.5:c.*285G>T
|
ENSP00000462599.1:n.*285G>T
|
|
ENST00000582005.5:c.*476G>T
|
ENSP00000462002.1:n.*476G>T
|
|
ENST00000582761.1:c.324G>T
|
ENSP00000462909.1:p.Leu108=
|
|
ENST00000584865.5:n.502G>T
|
|
|
NM_000789.3:c.2556G>T
|
NP_000780.1:p.Leu852=
|
|
NM_001178057.1:c.834G>T
|
NP_001171528.1:p.Leu278=
|
|
NM_152830.2:c.834G>T
|
NP_690043.1:p.Leu278=
|
|
XM_005257110.1:c.2007G>T
|
XP_005257167.1:p.Leu669=
|
|
XM_006721737.2:c.894G>T
|
XP_006721800.2:p.Leu298=
|
|
XM_006721737.3:c.894G>T
|
XP_006721800.2:p.Leu298=
|
|
NM_000789.4:c.2556G>T
MANE Select
|
NP_000780.1:p.Leu852=
|
|
NM_001178057.2:c.834G>T
|
NP_001171528.1:p.Leu278=
|
|
NM_152830.3:c.834G>T
|
NP_690043.1:p.Leu278=
|
|
NM_001382700.1:c.1989G>T
|
NP_001369629.1:p.Leu663=
|
|
NM_001382701.1:c.1704G>T
|
NP_001369630.1:p.Leu568=
|
|
NM_001382702.1:c.379+256G>T
|
NP_001369631.1:n.379+256G>T
|
|
NR_168483.1:n.934G>T
|
|
|