ENST00000636937.2:c.2504G>C
|
ENSP00000516154.1:p.Gly835Ala
|
|
ENST00000268124.11:c.2504G>C
MANE Select
|
ENSP00000268124.5:p.Gly835Ala
|
|
ENST00000530292.3:c.2105G>C
|
ENSP00000432885.2:p.Gly702Ala
|
|
ENST00000635986.2:c.2504G>C
|
ENSP00000490653.2:p.Gly835Ala
|
|
ENST00000636774.1:c.*1071G>C
|
ENSP00000489799.1:n.*1071G>C
|
|
ENST00000637238.1:c.1201G>C
|
ENSP00000490756.1:n.1201G>C
|
|
ENST00000637264.1:c.1576G>C
|
|
|
ENST00000666746.1:c.2081G>C
|
|
|
ENST00000670281.1:c.800+132G>C
|
ENSP00000499709.1:n.800+132G>C
|
|
ENST00000672071.1:n.2702G>C
|
|
|
ENST00000672923.2:n.2446G>C
|
|
|
ENST00000268124.9:c.2504G>C
|
ENSP00000268124.5:p.Gly835Ala
|
|
ENST00000442287.6:c.2504G>C
|
ENSP00000399851.2:p.Gly835Ala
|
|
ENST00000528881.2:c.196-570G>C
|
|
|
ENST00000530715.5:c.185+912G>C
|
ENSP00000431395.1:n.185+912G>C
|
|
ENST00000532584.5:n.653G>C
|
|
|
ENST00000631044.2:c.*1928G>C
|
ENSP00000486730.1:n.*1928G>C
|
|
NM_001126131.1:c.2504G>C
|
NP_001119603.1:p.Gly835Ala
|
|
NM_002693.2:c.2504G>C
|
NP_002684.1:p.Gly835Ala
|
|
NM_001126131.2:c.2504G>C
|
NP_001119603.1:p.Gly835Ala
|
|
NM_002693.3:c.2504G>C
MANE Select
|
NP_002684.1:p.Gly835Ala
|
|