ENST00000491302.2:n.1543G>C
|
|
|
ENST00000697630.1:n.6320G>C
|
|
|
ENST00000697631.1:c.2205G>C
|
ENSP00000513363.1:p.Leu735Phe
|
|
ENST00000697632.1:c.1452G>C
|
ENSP00000513364.1:p.Leu484Phe
|
|
ENST00000697633.1:c.1097G>C
|
|
|
ENST00000348564.11:c.2007G>C
|
ENSP00000306782.7:p.Leu669Phe
|
|
ENST00000442510.8:c.2490G>C
MANE Select
|
ENSP00000411355.3:p.Leu830Phe
|
|
ENST00000348564.10:c.2007G>C
|
ENSP00000306782.7:p.Leu669Phe
|
|
ENST00000442510.6:c.2490G>C
|
ENSP00000411355.3:p.Leu830Phe
|
|
NM_002838.4:c.2490G>C
|
NP_002829.3:p.Leu830Phe
|
|
NM_080921.3:c.2007G>C
|
NP_563578.2:p.Leu669Phe
|
|
XM_006711472.2:c.2346G>C
|
XP_006711535.1:p.Leu782Phe
|
|
XM_006711473.2:c.2292G>C
|
XP_006711536.1:p.Leu764Phe
|
|
XM_006711474.2:c.2148G>C
|
XP_006711537.1:p.Leu716Phe
|
|
XM_006711472.4:c.2346G>C
|
XP_006711535.1:p.Leu782Phe
|
|
XM_006711473.3:c.2292G>C
|
XP_006711536.1:p.Leu764Phe
|
|
XM_006711474.3:c.2148G>C
|
XP_006711537.1:p.Leu716Phe
|
|
NM_002838.5:c.2490G>C
MANE Select
|
NP_002829.3:p.Leu830Phe
|
|
NM_080921.4:c.2007G>C
|
NP_563578.2:p.Leu669Phe
|
|