ENST00000698881.1:c.1215G>C
|
ENSP00000514003.1:p.Leu405Phe
|
|
ENST00000418331.7:c.873G>C
MANE Select
|
ENSP00000400010.2:p.Leu291Phe
|
|
ENST00000418331.6:c.873G>C
|
ENSP00000400010.2:p.Leu291Phe
|
|
ENST00000440289.6:c.873G>C
|
ENSP00000409733.2:p.Leu291Phe
|
|
ENST00000613246.4:c.873G>C
|
ENSP00000477933.1:p.Leu291Phe
|
|
ENST00000615445.4:c.873G>C
|
ENSP00000479342.1:p.Leu291Phe
|
|
NM_001098503.1:c.873G>C
|
NP_001091973.1:p.Leu291Phe
|
|
NM_002843.3:c.873G>C
|
NP_002834.3:p.Leu291Phe
|
|
XM_011520249.1:c.906G>C
|
XP_011518551.1:p.Leu302Phe
|
|
XR_930883.1:n.1223G>C
|
|
|
XM_017018083.1:c.951G>C
|
XP_016873572.1:p.Leu317Phe
|
|
XM_017018084.1:c.894G>C
|
XP_016873573.1:p.Leu298Phe
|
|
XM_017018085.1:c.825G>C
|
XP_016873574.1:p.Leu275Phe
|
|
XR_930883.2:n.1282G>C
|
|
|
NM_002843.4:c.873G>C
MANE Select
|
NP_002834.3:p.Leu291Phe
|
|
NM_001098503.2:c.873G>C
|
NP_001091973.1:p.Leu291Phe
|
|