ENST00000684993.1:n.132G>T
|
|
|
ENST00000689018.1:n.41-1196G>T
|
|
|
ENST00000689809.1:c.73G>T
|
ENSP00000510752.1:p.Glu25Ter
|
|
ENST00000691867.1:c.73G>T
|
ENSP00000510706.1:p.Glu25Ter
|
|
ENST00000607778.2:c.73G>T
MANE Select
|
ENSP00000476100.1:p.Glu25Ter
|
|
ENST00000648328.1:c.*38G>T
|
ENSP00000497338.1:n.*38G>T
|
|
ENST00000607778.1:c.73G>T
|
ENSP00000476100.1:p.Glu25Ter
|
|
NM_207118.2:c.73G>T , LRG_469t1:c.73G>T
|
NP_997001.1:p.Glu25Ter
|
|
XM_017010862.1:c.103G>T
|
XP_016866351.1:p.Glu35Ter
|
|
NM_207118.3:c.73G>T
MANE Select
|
NP_997001.1:p.Glu25Ter
|
|