ENST00000542639.6:c.436G>T
|
ENSP00000440846.1:p.Ala146Ser
|
|
ENST00000686683.1:c.145G>T
|
ENSP00000509063.1:p.Ala49Ser
|
|
ENST00000686980.1:n.967G>T
|
|
|
ENST00000688006.1:c.436G>T
|
ENSP00000510311.1:p.Ala146Ser
|
|
ENST00000688859.1:n.391G>T
|
|
|
ENST00000689087.1:c.436G>T
|
ENSP00000508997.1:p.Ala146Ser
|
|
ENST00000693128.1:c.730G>T
|
ENSP00000508493.1:p.Ala244Ser
|
|
ENST00000338702.4:c.835G>T
MANE Select
|
ENSP00000340684.3:p.Ala279Ser
|
|
ENST00000338702.3:c.835G>T
|
ENSP00000340684.3:p.Ala279Ser
|
|
ENST00000542639.5:c.436G>T
|
ENSP00000440846.1:p.Ala146Ser
|
|
NM_000240.3:c.835G>T
|
NP_000231.1:p.Ala279Ser
|
|
NM_001270458.1:c.436G>T
|
NP_001257387.1:p.Ala146Ser
|
|
NM_000240.4:c.835G>T
MANE Select
|
NP_000231.1:p.Ala279Ser
|
|
NM_001270458.2:c.436G>T
|
NP_001257387.1:p.Ala146Ser
|
|