ENST00000636937.2:c.3310T>G
|
ENSP00000516154.1:p.Ser1104Ala
|
|
ENST00000268124.11:c.3310T>G
MANE Select
|
ENSP00000268124.5:p.Ser1104Ala
|
|
ENST00000530292.3:c.2911T>G
|
ENSP00000432885.2:p.Ser971Ala
|
|
ENST00000635986.2:c.*380T>G
|
ENSP00000490653.2:n.*380T>G
|
|
ENST00000636774.1:c.*1877T>G
|
ENSP00000489799.1:n.*1877T>G
|
|
ENST00000637238.1:c.2119T>G
|
ENSP00000490756.1:n.2119T>G
|
|
ENST00000637264.1:c.2382T>G
|
|
|
ENST00000666746.1:c.2887T>G
|
|
|
ENST00000672071.1:n.3508T>G
|
|
|
ENST00000672695.1:n.487T>G
|
|
|
ENST00000672923.2:n.3310T>G
|
|
|
ENST00000268124.9:c.3310T>G
|
ENSP00000268124.5:p.Ser1104Ala
|
|
ENST00000442287.6:c.3310T>G
|
ENSP00000399851.2:p.Ser1104Ala
|
|
ENST00000530292.2:c.394T>G
|
ENSP00000432885.1:p.Ser132Ala
|
|
ENST00000631044.2:c.*2734T>G
|
ENSP00000486730.1:n.*2734T>G
|
|
NM_001126131.1:c.3310T>G
|
NP_001119603.1:p.Ser1104Ala
|
|
NM_002693.2:c.3310T>G
|
NP_002684.1:p.Ser1104Ala
|
|
NM_001126131.2:c.3310T>G
|
NP_001119603.1:p.Ser1104Ala
|
|
NM_002693.3:c.3310T>G
MANE Select
|
NP_002684.1:p.Ser1104Ala
|
|