ENST00000682587.1:c.2638C>T
(SYNGAP1)
|
ENSP00000507403.1:p.His880Tyr
|
|
ENST00000418600.7:c.2896C>T
(SYNGAP1)
|
ENSP00000403636.3:p.His966Tyr
|
|
ENST00000449372.7:c.2854C>T
(SYNGAP1)
|
ENSP00000416519.4:p.His952Tyr
|
|
ENST00000629380.3:c.2896C>T
(SYNGAP1)
|
ENSP00000486463.1:p.His966Tyr
|
|
ENST00000644458.1:c.2896C>T
(SYNGAP1)
|
ENSP00000495541.1:p.His966Tyr
|
|
ENST00000645250.1:c.2719C>T
(SYNGAP1)
|
ENSP00000494861.1:p.His907Tyr
|
|
ENST00000646630.1:c.2896C>T
(SYNGAP1)
MANE Select
|
ENSP00000496007.1:p.His966Tyr
|
|
ENST00000293748.9:c.2851C>T
(SYNGAP1)
|
ENSP00000293748.6:p.His951Tyr
|
|
ENST00000418600.6:c.2896C>T
(SYNGAP1)
|
ENSP00000403636.3:p.His966Tyr
|
|
ENST00000428982.4:c.2719C>T
(SYNGAP1)
|
ENSP00000412475.2:p.His907Tyr
|
|
ENST00000449372.6:c.2854C>T
(SYNGAP1)
|
ENSP00000416519.3:p.His952Tyr
|
|
ENST00000628646.2:c.2896C>T
(SYNGAP1)
|
ENSP00000486431.1:p.His966Tyr
|
|
ENST00000629380.2:c.2896C>T
(SYNGAP1)
|
ENSP00000486463.1:p.His966Tyr
|
|
NM_006772.2:c.2896C>T
(SYNGAP1)
|
NP_006763.2:p.His966Tyr
|
|
NM_001130066.1:c.2854C>T
(SYNGAP1)
|
NP_001123538.1:p.His952Tyr
|
|
NM_001130066.2:c.2854C>T
(SYNGAP1)
|
NP_001123538.1:p.His952Tyr
|
|
NM_006772.3:c.2896C>T
(SYNGAP1)
MANE Select
|
NP_006763.2:p.His966Tyr
|
|
NR_174954.1:n.329+3158G>A
(SYNGAP1-AS1)
|
|
|