ENST00000346342.8:c.954G>C
MANE Select
|
ENSP00000329546.4:p.Leu318Phe
|
|
ENST00000346342.7:c.954G>C
|
ENSP00000329546.3:p.Leu318Phe
|
|
ENST00000375581.3:c.1020G>C
|
ENSP00000364731.3:p.Leu340Phe
|
|
ENST00000541084.5:c.768G>C
|
ENSP00000442051.2:p.Leu256Phe
|
|
NM_000131.4:c.1020G>C , LRG_554t1:c.1020G>C
|
NP_000122.1:p.Leu340Phe
|
|
NM_001267554.1:c.768G>C
|
NP_001254483.1:p.Leu256Phe
|
|
NM_019616.3:c.954G>C , LRG_554t2:c.954G>C
|
NP_062562.1:p.Leu318Phe
|
|
NR_051961.1:n.1041G>C
|
|
|
XM_006719963.2:c.813G>C
|
XP_006720026.1:p.Leu271Phe
|
|
XM_011537474.1:c.1062G>C
|
XP_011535776.1:p.Leu354Phe
|
|
XM_011537475.1:c.876G>C
|
XP_011535777.1:p.Leu292Phe
|
|
XM_011537476.1:c.714G>C
|
XP_011535778.1:p.Leu238Phe
|
|
XM_011537477.1:c.1023G>C
|
XP_011535779.1:p.Leu341Phe
|
|
XM_006719963.3:c.858G>C
|
XP_006720026.2:p.Leu286Phe
|
|
XM_011537474.2:c.1107G>C
|
XP_011535776.2:p.Leu369Phe
|
|
XM_011537475.2:c.921G>C
|
XP_011535777.2:p.Leu307Phe
|
|
XM_011537476.2:c.714G>C
|
XP_011535778.1:p.Leu238Phe
|
|
NM_019616.4:c.954G>C
MANE Select
|
NP_062562.1:p.Leu318Phe
|
|
NR_051961.2:n.1038G>C
|
|
|
NM_001267554.2:c.768G>C
|
NP_001254483.1:p.Leu256Phe
|
|