ENST00000356392.9:c.918G>A
MANE Select
|
ENSP00000348757.3:p.Lys306=
|
|
ENST00000356392.8:c.918G>A
|
ENSP00000348757.3:p.Lys306=
|
|
ENST00000586836.5:c.345G>A
|
ENSP00000467429.1:p.Lys115=
|
|
ENST00000591179.5:c.738G>A
|
ENSP00000466800.1:p.Lys246=
|
|
ENST00000591345.5:c.*837G>A
|
ENSP00000467313.1:n.*837G>A
|
|
NM_001302453.1:c.756G>A
|
NP_001289382.1:p.Lys252=
|
|
NM_001302454.1:c.738G>A
|
NP_001289383.1:p.Lys246=
|
|
NM_145045.4:c.918G>A
|
NP_659482.3:p.Lys306=
|
|
XM_017026241.1:c.904+14G>A
|
XP_016881730.1:n.904+14G>A
|
|
NM_145045.5:c.918G>A
MANE Select
|
NP_659482.3:p.Lys306=
|
|
NM_001302454.2:c.738G>A
|
NP_001289383.1:p.Lys246=
|
|